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Amg

FDA UDI

Class I (US FDA UDI)

by Arrow Medsource Group Limited

Identity

Trade Name
AMG FDA UDI
Generic Name
Shoe cover FDA UDI
Model / Reference
BC0001 FDA UDI

Identifiers

Primary DI / UDI-DI
00850017650695 FDA UDI
FDA Product Code
BWP FDA UDI
GMDN Term
Shoe cover FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 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

No

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: Shoe cover

Amg by Arrow Medsource Group Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Shoe cover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bc743a4c-ce0a-4b40-9daf-0479baf7ecad 32 fields · synced Jun 6, 2026