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Home> Company News> Reusable Disinfection Requirements for Medical Rehabilitation Gel Pads and Pressure

Reusable Disinfection Requirements for Medical Rehabilitation Gel Pads and Pressure

2026,09,29

PRODUCT REQUIREMENTS

Reusable medical gel pads require: pressure-redistributing softness that does not bottom out; biocompatible non-irritating skin-contact chemistry; non-porous surface that does not absorb fluids or harbor contaminants; tolerance of quaternary ammonium, chlorine and alcohol disinfection without hardening or tack loss; FDA/LFGB and RoHS/REACH documentation with ISO 10993 support; dimensional stability over years of reuse; and easy clean-down between patients.

Liquid tank adhesive

CORRESPONDING PRODUCT MODEL PARAMETERS

Recommended model: HY-9409 - Transparent low-tack grade for intimate apparel, personal-care and body-contact products requiring clarity and skin-safe materials

Model

Color

Viscosity (mPa.s)

Operation Time (min)

Cure Time (hr)

Penetration (0.1mm)

Tack

Mix Ratio

Density (g/cm3)

HY-9409

Transparent

2200+/-400

20-40

4-6

150+/-30

Low

1:1

0.96

GRADE SELECTION GUIDE

Model

Color

Penetration (0.1mm)

Tack

Typical Applications

HY-9400

Blue

200

High

HEPA/ULPA filter gel channels, biosafety cabinet seals, applications requiring strong adhesion and re-sealability

HY-9405

Blue

170

Medium

Electronic potting, sensor encapsulation, applications balancing softness and dimensional stability

HY-9409

Transparent

150

Low

Transparent gel pads, intimate apparel, prosthetic devices, applications requiring visual clarity or easy repositioning

FREQUENTLY ASKED QUESTIONS

Q: Can gel pads be disinfected between patients?

A: Yes. The non-porous cured gel tolerates quaternary ammonium, chlorine and alcohol disinfectants per hospital protocol; pads are typically also film-covered, and no fluid is absorbed.

Q: Does the gel prevent pressure injuries better than foam?

A: Gel redistributes pressure without bottoming out and does not take compression set, so it maintains protection over years of reuse, unlike foam that compacts.

Q: What biocompatibility documentation is available?

A: FDA 21 CFR 177.2600 and LFGB reports are standard; ISO 10993 cytotoxicity, sensitization and irritation testing can be coordinated for medical-device registration.

 

QUALITY ASSURANCE & CERTIFICATION

Every batch of Hong Ye HY-94 series jelly gel is produced under ISO 9001 certified quality management in a dedicated silicone workshop, with incoming raw-material inspection, in-process mixing control and finished-product testing on every batch. Before release each lot is checked for viscosity, mix ratio, cure time, penetration, color and tack, and a Certificate of Analysis (COA) listing the actual measured values ships with every order. Standard grades carry RoHS 2.0 and REACH SVHC test reports; skin-contact and baby-care grades can be supplied with FDA 21 CFR 177.2600 and LFGB Section 30/31 reports and, on request, ISO 10993 biocompatibility testing; flame-retardant grades meet UL94 V-0. Food-contact, medical and export orders are supported by the corresponding compliance files for customer qualification. Hong Ye has manufactured and supplied jelly gel to contractors, filter builders and equipment makers in over 60 countries since 2005, with monthly capacity above 500 tons, batch traceability and multi-language documentation. Application engineers provide grade selection, sample evaluation, on-site or video pouring guidance and after-sales follow-up, and technical data sheets (TDS), safety data sheets (SDS) and test reports are available before order to support tender and audit processes.

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CONCLUSION

The market for tank sealant jelly gel in this application area continues to expand as cleanroom construction, electronic encapsulation, automotive electrification, energy storage and consumer product manufacturing drive demand for reliable two-component addition-cure silicones. Hong Ye supports this growth with ISO 9001 certified production, 500-plus ton monthly capacity, complete compliance documentation and responsive application engineering. Buyers evaluating suppliers are advised to look beyond unit price and compare batch-to-batch consistency, documentation completeness, delivery stability and technical service responsiveness, because the cost of a sealing or potting failure - rework, downtime, certification delay or product recall - far exceeds the incremental cost of a quality gel. Choosing the correct grade for the channel, operating temperature and service environment, following the 1:1 mixing and pouring procedure and validating with a small trial batch all help secure a durable seal. Hong Ye welcomes sample requests and application enquiries; our engineers will recommend the HY-9400, HY-9405 or HY-9409 grade that matches the sealing or potting requirement and support qualification from first sample through volume production.

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Ms. zhou

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alice@szrl.net

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