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Texwipe STX1721 Sterile Revolve AlphaMop Polyester Cleanroom Replacement Mop Covers (Refills)

Texwipe STX1721 Sterile Revolve AlphaMop Polyester Cleanroom Replacement Mop Covers (Refills)

$1,040.91
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SKU:
STX1721
Availability:
7 - 10 Business Days
Shipping:
Calculated at Checkout
Quantity Option (Case):
100 Mop Covers Per Case (10 Bags of 10 Mop Covers)
Type:
Dry Mop
Sterile:
Yes
Texwipe STX1721 Revolve™ AlphaMop™ Sterile Integrated Mop Covers/Pads — 15" x 8" System Fit, Triple-Bagged (100/Case)
STX1721 is a sterile, cover/pad-integrated replacement for Texwipe AlphaMop™ 15" x 8" flat mop heads (such as TX7108 / TX7108AH). It is designed for technician-driven, contamination-controlled cleaning: applying and removing disinfectants/cleaners, routine surface cleaning of floors/walls/ceilings, and spill control in critical environments. Revolve™ integrated construction eliminates the separate pad step — you replace the entire wiping surface as a single unit to reduce handling time and support strict “change often” mop discipline.

For over 35 years, SOS and Texwipe have been close partners, and SOSCleanroom is the authorized Master Distributor of ITW Texwipe for the United States market. That relationship matters when you are standardizing cleanroom mops and refills: it supports continuity of supply, stable product lineage, and fast access to the manufacturer documentation your QA/QC team expects.
Published configuration (STX1721)
  • Format: Revolve™ integrated cover/pad (no separate pad required)
  • System fit: Sized to fit 15" x 8" flat mop heads (AlphaMop™ platform)
  • Material: 100% upcycled polyester (Revolve™ sustainable product line)
  • Sterile: Yes (gamma irradiated; Sterility Assurance Level (SAL) 10-6 per AAMI guidance)
  • Packaging: 100 covers per case (10 bags of 10 covers), triple-bagged
  • Cleanroom environments (as published): ISO Class 3–7; EU Grade A–D
  • Temperature limit (as published): Appropriate for use with temperatures less than 400°F (205°C)
  • Shelf life (as published): Sterile — 3 years from date of manufacture
Low-linting intent — and the reality check
STX1721 is engineered for critical cleaning with Revolve™ processing intended to support low levels of ions, non-volatile residues (NVRs), particles and fibers for use in critical cleaning applications and environments. Even so, no wiping/mopping textile is truly “zero-shedding” in every use condition. Treat each cover as a controlled consumable: stage it correctly, change it often, and avoid over-wetting or abrasive contact that can elevate particle release and streaking.
Practical cleanroom use guidance (technicians and engineers)
  • Bag-in discipline (sterile suites): Use the triple-bag layers intentionally. De-bag to the appropriate grade boundary per site CCS/SOP; only the final bag should enter the highest-grade area. Do not stage opened bags on work surfaces.
  • One cover, one zone (recommended practice): Assign one cover per room/zone/step to reduce cross-contamination. When moving from “dirtier” to “cleaner” areas, change the cover before crossing the boundary.
  • Pre-wet control: If your SOP requires pre-wetting, wet the cover evenly (do not spot-soak). Uneven wetting causes streaks, incomplete disinfectant contact, and residue islands.
  • Wringing consistency: Use a validated wringing method (wringer or controlled hand pressure) to avoid over-wet floors and excessive residue. Over-wet mops are a common root cause of sticky residue and slip hazards.
  • Stroke mechanics: Use slow, overlapping strokes with consistent edge-leading orientation. Avoid aggressive scrubbing; let chemistry and dwell time do the work, then remove residues with controlled passes.
  • Change frequency: Change the cover at defined intervals (time, area, or visible soil/load). If the cover begins to drag, streak, or shed, treat it as “loaded” and replace immediately.
Compatibility and solution-use notes (publish-what-is-known)
  • Common solvents/cleaners (as published): Suitable for cleaning with solvents such as isopropyl alcohol (IPA), ethanol, acetone, and degreasers.
  • Disinfectant application: Designed for applying and removing solutions including disinfectants. Verify dwell time and residue-removal steps under your SOP.
  • Autoclave: Autoclave safe is indicated for the Revolve™ integrated cover/pad family. If your program depends on autoclave cycling, qualify the cover under your specific cycle parameters and inspect for deformation, streaking, and residue behavior before standardization.
  • High-oxidizer chemistries: Not published for STX1721 as a specific compatibility claim. If your rotation includes strong oxidizers (e.g., peroxide/peracetic blends), qualify the cover for sorption, mechanical integrity, and residue carryover under your conditions.
Sterility, packaging layers, and documentation control
This section is written for facilities that operate under contamination control strategies (CCS) and audit-driven documentation expectations.
Control point What STX1721 provides (published) Technician note
Sterility assurance Gamma irradiated; SAL 10-6 (AAMI guidance) Do not compromise the bag layers; treat any puncture/tear as non-sterile.
Packaging layers Triple-bagged (10 bags of 10 covers per case) Use staged de-bag per grade boundary; do not “carry open bags” between rooms.
Certificates / traceability Certificates of Compliance, Analysis, and Processing/Irradiation available (per manufacturer) Capture lot/expiry in your logbook or eQMS at point-of-use, not after the shift.
Shelf life Sterile — 3 years from date of manufacture Rotate stock FIFO; never “borrow” expired sterile covers for non-sterile tasks in controlled zones.
Annex 1 alignment notes (risk-based cleaning programs)
EU GMP Annex 1 emphasizes a contamination control strategy (CCS) and expects cleaning/disinfection practices to be designed, justified, and controlled — including rotation and residue management where applicable. STX1721 supports those programs by enabling frequent surface changes, sterile-ready packaging layers, and documentation access for qualification.
Annex 1 program expectation How to operationalize with STX1721 What to document
CCS: defined controls for contamination risk reduction Define cover change frequency by zone/area/time; enforce “single-use per zone” where required. Cover lot/expiry, room/zone, chemistry used, operator, start/finish time.
Validated cleaning/disinfection: residue control and removal Avoid over-wetting; use controlled wringing and defined strokes; include a residue-removal pass if your chemistry requires it. Dwell time adherence, residue removal step, and any post-clean inspection results.
Rotation/sporicidal use (where required by risk profile) Use a fresh cover for sporicidal steps; do not carry sporicidal residues into non-sporicidal zones. Chemistry rotation schedule, contact times, and any neutralization/residue management requirements.
Common failure modes 
  • Streaking / residue film: Most often from over-wetting, inconsistent wringing, or chemistry that requires a defined residue-removal step. Control liquid load and follow your validated rinse/wipe sequence.
  • Cross-contamination between rooms: Happens when a “still looks clean” cover is carried across boundaries. Fix with one-cover-per-zone discipline and boundary change points.
  • Incomplete disinfectant contact: Caused by dry spots, fast strokes, or skipping dwell time. Fix with even wetting, slower strokes, and dwell time timing.
  • Particle shedding events: Can be triggered by abrasive floor debris, aggressive scrubbing, or dragging a loaded cover. Fix by pre-picking debris (as permitted), changing covers sooner, and avoiding “grinding” action.
  • Packaging breach / sterility loss: Small punctures, tears, or wet bags can compromise sterile introduction. Reject damaged packs immediately and record the deviation per SOP.
  • Static attraction (dry environments): Covers can attract fines when rubbed against garments or when used too dry. Follow site ESD/grounding controls and maintain controlled wetting.
Storage and handling best practices
  • Keep covers sealed in original packaging until point-of-use; stage only what will be consumed in the current operation.
  • Store in a clean, dry area to prevent bag condensation and to protect sterile packaging integrity.
  • Use FIFO and verify expiry before entry into higher-grade areas.
  • After use, discard as contaminated consumables per your facility waste stream rules (especially after sporicidal steps).
Documentation 
SOS-hosted Texwipe AlphaMop™ Series TDS (includes STX1721 line item): Click Here
Texwipe AlphaMop™ Series TDS (manufacturer PDF): Click Here
Texwipe manufacturer page (STX1721): Click Here
Revolve™ Mop Covers TDS (manufacturer PDF): Click Here
SOS-hosted Revolve™ TechNote (background and processing context): Click Here
SOS-hosted Revolve™ Q&A (qualification and sustainability discussion): Click Here
EU GMP Annex 1 (Manufacture of Sterile Medicinal Products) — reference document: Click Here
If you have any questions please email us at Sales@SOSsupply.com or give us a call at (214)340-8574.

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Last updated: January 9, 2026
© 2026 SOS Supply. All rights reserved.
The Technical Vault Sterile Sustainable Floor Mopping Discipline (Upcycled Polyester) (Applied Use Case: Texwipe™ STX1721 Sterile Revolve® AlphaMop® Polyester Cleanroom Replacement Mop Covers — Refills)

Purpose & Scope

The STX1721 are sterile replacement mop covers for the AlphaMop® platform, manufactured using Revolve® upcycled polyester. In sterile housekeeping, sustainability is only valuable if it preserves control. This entry focuses on how to keep Revolve® floor mopping repeatable through sterile handling, controlled wetting, unidirectional lanes, and objective change-out triggers—so “green” never becomes “variable.”

Visual Aids (Technique, Zoning, Lifecycle)

Use this graphic to reinforce clean-to-less-clean sequencing, zone discipline, and consumable lifecycle control. Revolve® covers should follow the same SOP controls as any sterile mop cover.

Cleanroom mopping technique, cleanroom zoning floor map concept, and mop cover lifecycle diagram

Implementation note: Sustainability goals should never relax zone boundaries, wetness control, or change-out triggers.

Sterile Handling (Keep “Sterile Intent” Intact)

The most common sterile housekeeping deviation is setup transfer: sterile covers handled with gloves that have already touched non-sterile surfaces (cart rails, bucket exteriors, door hardware, gown sleeves). A defensible SOP defines how covers are opened and seated without touch contamination.

  • Open at point-of-use: avoid staging opened sterile packs.
  • No staging on surfaces: do not set covers on counters, bucket rims, or carts.
  • Glove transfer control: define what happens if gloves touch non-sterile items during setup.
  • Defined removal/disposal: remove and discard used covers without contacting clean tools or packaging.

Revolve® (Upcycled Polyester) in Aseptic Cleaning: The Defensible Approach

In regulated environments, what matters is the finished product’s suitability and the validated facility process. The operational risk is not the sustainability story—it’s process drift (extended use, cross-zone carryover, inconsistent wetting, and “touch up” behavior). Keep controls unchanged and documentation simple.

  • Same controls, same SOP: treat Revolve® covers like standard sterile mop covers (no relaxed rules).
  • Zone dedication stays strict: sustainability should not justify moving media between zones.
  • Objective change-outs: keep triggers performance-based and audit-ready.

Controlled Wetting (Uniform Coverage Prevents Streaking)

Floor mopping is most repeatable when covers are uniformly wetted and used in a defined lane pattern. Over-wetting increases drip/splash transfer and can drive streaking or residue. Under-wetting increases friction and encourages scrubbing.

  • Even wetting: avoid wet “hot spots” that print into lanes.
  • Drip control: if it drips in transit, wring/reload per SOP.
  • First-pass planning: initial contact can be wetter—define where that first lane begins.

Technique: Unidirectional Lanes (Clean-to-Less-Clean)

In aseptic programs, unidirectional lanes are commonly used to reduce re-contact and make coverage verifiable. The goal is controlled overlap and planned sequencing—not backtracking “touch ups.”

  • Align with zoning: start in the cleanest defined area and work outward per your SOP.
  • Consistent overlap: keep overlap consistent and visible; avoid random passes.
  • No backtracking: don’t drag used media backward to correct a missed spot—change media if needed.
  • Edge discipline: manage perimeters separately to avoid pulling residues inward.

Objective Change-Out Triggers (Sterile Revolve® Floor Covers)

Keep change-outs objective so sustainability goals don’t quietly extend use windows. Sterile floor covers can look “fine” while already loaded with residues.

  • Change by zone boundary: do not carry used covers into cleaner zones.
  • Change by task stage: perimeter/entry work should not share media with critical interiors.
  • Change by performance: streaking/haze onset, increased drag, reduced pickup response, visible loading.
  • Change by handling event: dropped cover, torn package, uncontrolled staging, touch contamination.

Details Most Websites Skip (Sustainability Without Process Drift)

  • Don’t “stretch” sterile consumables: environmental goals should not dilute audit defensibility.
  • Document what doesn’t change: the SOP controls (zoning, lanes, wetness, change-outs) remain the same.
  • Rest-point control: define where mop heads may be staged during pauses to prevent recontact and transfer.
  • Troubleshooting order: new cover + fresh solution + clean tool surfaces before changing chemistry.

SOP & Audit Readiness Checklist (Sterile Revolve® Floor Covers)

  • Define sterile staging and opening-at-point-of-use rules.
  • Define glove management for handling/seating covers (transfer prevention).
  • Define loading targets (uniform wetting; drip control; first-pass planning).
  • Define lane technique (direction, overlap, edge control, no backtracking).
  • Define objective change-out triggers (zone boundaries, stages, performance signals, handling events).

Disclaimer: This Technical Vault content is provided for educational purposes only. Manufacturer instructions, facility SOPs, disinfectant label directions (including contact times), and site-specific risk assessments must always take precedence. Sterile housekeeping programs must follow validated procedures for entry, handling, and documentation per your quality system.

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