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Resilient Medical Solutions

FDA UDI

Class I (US FDA UDI)

by Resilient Medical Solutions, LLC

Identity

Trade Name
Resilient Medical Solutions FDA UDI
Generic Name
Woven gauze pad, non-antimicrobial FDA UDI
Device Name
12-Ply USP Type VII Gauze Sponge, 4x4, Non-Sterile FDA UDI
Model / Reference
RMWC2 FDA UDI
Description
12-Ply USP Type VII Gauze Sponge, 4x4, Non-Sterile FDA UDI

Identifiers

Primary DI / UDI-DI
00850037100606 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Woven gauze pad, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Woven gauze pad, non-antimicrobial

A non-medicated device in the form of a patch or swab made from woven material primarily designed to absorb fluids for medical purposes. It is typically used to clean, cover, or pack wounds or abrasions and absorb their exudates. This single-use device is implantable: false. The device has been tested for safety and does not contain MRI Safety Information. The company producing this product is Resilient Medical Solutions, LLC. This product is labeled as non-marketable retail (NRL).

Similar devices

Also classified as Woven gauze pad, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ed7c6b2a-7b74-492b-b609-954a428fa371 33 fields · synced Jul 11, 2026