SOS Cleanroom Texwipe TX3340 TOC Kit Cleaning Validation for 12 Samples - Case

Product Description

Texwipe TX3340 is a controlled, audit-friendly TOC (Total Organic Carbon) cleaning validation sampling kit built to reduce background contribution from the sampling tools so your results reflect the surface—not the vial, cap, label, or swab. Each kit is designed for surface sampling as part of a formal cleaning validation protocol and includes pre-washed low-TOC vials, low-TOC polyester knit sampling swabs (TX714K), and cleanroom-compatible labels organized in a cleanroom-compatible polypropylene transport box. The TX714K snap swab uses a notched, break-away handle to minimize touch points and support repeatable transfer of the swab head into the vial with reduced handling variability. The swab head is double-layer, double-knit polyester knit for controlled pickup and release into diluent during analysis (and is low-linting in use, though no swab or wiper is truly ‘lint-free’ in every process condition).

• SKU: TX3340 KIT
• Kit configuration: 12 vials with 12 blank labels and 24 (TX714K) swabs per kit
• Case configuration: 18 kits per case
• Swab family: TOC Validation
• Swab type: Dry swab (kit-based sampling system)
• Swab material: Polyester (double-layer, double-knit polyester head) with polypropylene handle
• Certified TOC background (swabs): <50 µg/L (<50 ppb) TOC (typical certification level for TX714K kit swabs)
• Certified TOC background (vials): <10 µg/L (<10 ppb) TOC (typical certification level for kit vials)
• Vials: 40 mL clear vials with bonded septa caps; one-piece cap-and-septum design; polyethylene overcap; sloped shoulder design to reduce headspace
• Packaging: Components organized in a cleanroom-compatible polypropylene box; supplied double-bagged
• Analyzer/program fit: Designed for TOC-based cleaning validation workflows and commonly positioned as compatible with major TOC analyzer programs (confirm fit to your validated method and lab SOP)
• Shelf life: 5 years (program guidance; confirm at receipt and per your internal quality system)
• Use environments: Commonly used in regulated pharmaceutical/biotech and other controlled sampling workflows where low-background swab sampling supports validated cleaning verification (final suitability depends on your method, diluent, and SOP)