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Birkova

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
Birkova FDA UDI
Generic Name
Stretcher mattress FDA UDI
Device Name
Stretcher Pad - Gendron 890 - 76-inch x 28-inch x 4-inch FDA UDI
Model / Reference
Stretcher Pads FDA UDI
Description
Stretcher Pad - Gendron 890 - 76-inch x 28-inch x 4-inch FDA UDI

Identifiers

Catalog Number
SP5212 FDA UDI
Primary DI / UDI-DI
00724995206741 FDA UDI
FDA Product Code
LWG FDA UDI
GMDN Term
Stretcher mattress 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Stretcher mattress

Birkova by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stretcher mattress.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 8e278969-f624-4466-a98d-9086fa2cd6f0 35 fields · synced Jun 8, 2026