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Ritmed

FDA UDI

Class I (US FDA UDI)

by AMD Medicom Inc

Identity

Trade Name
Ritmed FDA UDI
Generic Name
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI
Device Name
Ritmed Tubular Mesh Bandage Roll - Length: 25 yd - Size: 8 (Medium Chest, Back and Axilla) FDA UDI
Model / Reference
51418-LF FDA UDI
Description
Ritmed Tubular Mesh Bandage Roll - Length: 25 yd - Size: 8 (Medium Chest, Back and Axilla) FDA UDI

Identifiers

Catalog Number
51418-LF FDA UDI
Primary DI / UDI-DI
10686864048746 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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: Skin treatment/dressing-supportive limb/finger bandage, single-use

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

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, single-use.

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 e840a7e2-1188-44af-8cfa-629e0afeb9e9 37 fields · synced Jun 8, 2026