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Aqualgel

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
AQUALGEL FDA UDI
Generic Name
Operating table patient pressure distribution pad, reusable FDA UDI
Device Name
Oasis Full Length Table Pad is flexible, durable full length overlay is suggested as a companion to the many other OASIS positioners for patients in supine, prone, and Trendelenburg postures. FDA UDI
Model / Reference
BF473 FDA UDI
Description
Oasis Full Length Table Pad is flexible, durable full length overlay is suggested as a companion to the many other OASIS positioners for patients in supine, prone, and Trendelenburg postures. FDA UDI

Identifiers

Catalog Number
BF473 FDA UDI
Primary DI / UDI-DI
00724995220167 FDA UDI
FDA Product Code
LWG FDA UDI
GMDN Term
Operating table patient pressure distribution pad, reusable 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Operating table patient pressure distribution pad, reusable

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

Similar devices

Also classified as Operating table patient pressure distribution pad, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI c2ccac4a-9502-4b2d-99d0-0897b6f9a308 36 fields · synced Jun 6, 2026