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Oasis

FDA UDI

Class I (US FDA UDI)

by Trulife Limited

Identity

Trade Name
Oasis FDA UDI
Generic Name
Operating table patient pressure distribution pad, reusable FDA UDI
Device Name
Oasis 3/4 Length Table Pad FDA UDI
Model / Reference
OA031G FDA UDI
Description
Oasis 3/4 Length Table Pad FDA UDI

Identifiers

Primary DI / UDI-DI
00643293029053 FDA UDI
FDA Product Code
JZR FDA UDI
GMDN Term
Operating table patient pressure distribution pad, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.4900 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Operating table patient pressure distribution pad, reusable

Oasis by Trulife Limited — 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
Trulife Limited

Sources (1)

  • FDA UDI 96e58580-6231-49e4-838e-9e05f86ed5f8 33 fields · synced Jun 7, 2026