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BIOS Living

FDA UDI

Class I (US FDA UDI)

by Thermor Ltd

Identity

Trade Name
BIOS Living FDA UDI
Generic Name
Bath back rest/seat FDA UDI
Device Name
Transfer Bench FDA UDI
Model / Reference
LF766 FDA UDI
Description
Transfer Bench FDA UDI

Identifiers

Primary DI / UDI-DI
00057475267667 FDA UDI
FDA Product Code
IKX FDA UDI
GMDN Term
Bath back rest/seat FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bath back rest/seat

BIOS Living by Thermor Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bath back rest/seat.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thermor Ltd

Sources (1)

  • FDA UDI 2f634d0f-9945-48f9-85bd-a8c0c4a94098 33 fields · synced May 31, 2026