← Back to catalogue

Ritmed All Gauze

FDA UDI

Class I (US FDA UDI)

by AMD Medicom Inc

Identity

Trade Name
RITMED ALL GAUZE FDA UDI
Generic Name
Woven gauze pad, non-antimicrobial FDA UDI
Device Name
RITMED ALL GAUZE SPONGE 16 PLY 4 X 4 Inch FDA UDI
Model / Reference
310040 FDA UDI
Description
RITMED ALL GAUZE SPONGE 16 PLY 4 X 4 Inch FDA UDI

Identifiers

Catalog Number
310040 FDA UDI
Primary DI / UDI-DI
10686864056468 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Woven gauze pad, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Woven gauze pad, non-antimicrobial

Ritmed All Gauze by AMD Medicom Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Woven gauze pad, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
AMD Medicom Inc

Sources (1)

  • FDA UDI f9c7c0b5-292c-4045-89a8-769bc99b9edb 37 fields · synced Jun 8, 2026