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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
Eye pad FDA UDI
Device Name
AMD-RITMED OVAL EYE PAD 2 1/8 X 2 5/8 Inch FDA UDI
Model / Reference
A1111 FDA UDI
Description
AMD-RITMED OVAL EYE PAD 2 1/8 X 2 5/8 Inch FDA UDI

Identifiers

Catalog Number
A1111 FDA UDI
Primary DI / UDI-DI
10686864050299 FDA UDI
FDA Product Code
HMP FDA UDI
GMDN Term
Eye pad FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4440 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: Eye pad

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

Similar devices

Also classified as Eye pad.

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 3473501d-57f9-450d-a0d9-cdb1c57ce5e7 37 fields · synced Jun 8, 2026