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Amd-Ritmed

FDA UDI

Class I (US FDA UDI)

by AMD Medicom Inc

Identity

Trade Name
AMD-RITMED FDA UDI
Generic Name
Surgical towel FDA UDI
Device Name
RITMED O.R. TOWEL - Prewashed - Blue - Sterile FDA UDI
Model / Reference
5004-B FDA UDI
Description
RITMED O.R. TOWEL - Prewashed - Blue - Sterile FDA UDI

Identifiers

Catalog Number
5004-B FDA UDI
Primary DI / UDI-DI
10686864021817 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Surgical towel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical towel

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

Similar devices

Also classified as Surgical towel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AMD Medicom Inc

Sources (1)

  • FDA UDI 73539bf4-f0f4-44e9-aa94-22117dc83aab 36 fields · synced May 31, 2026