Imperial Replacement mat

FDA UDI

Class I (US FDA UDI)

by Imperial Surgical Ltd

Identity

Trade Name: Imperial Replacement mat FDA UDI
Generic Name: Anti-fatigue floor mat FDA UDI
Device Name: Replacement Pad FDA UDI
Model / Reference: OR-36363-1A FDA UDI
Description: Replacement Pad FDA UDI

Identifiers

Catalog Number: OR-36363-1A FDA UDI
Primary DI / UDI-DI: 07540162040504 FDA UDI
FDA Product Code: FZM FDA UDI
GMDN Term: Anti-fatigue floor mat FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4950 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anti-fatigue floor mat

Imperial Replacement mat by Imperial Surgical Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Imperial Surgical Ltd

Sources (1)

FDA UDI 512d167a-a5ae-460e-8db4-1ca964f8b6fa 35 fields · synced Jun 6, 2026