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BIOS Living

FDA UDI

Class II (US FDA UDI)

by Thermor Ltd

Identity

Trade Name
BIOS Living FDA UDI
Generic Name
Patient lifting system bath chair FDA UDI
Device Name
Bath Lift FDA UDI
Model / Reference
59023 FDA UDI
Description
Bath Lift FDA UDI

Identifiers

Primary DI / UDI-DI
00057475590239 FDA UDI
FDA Product Code
FNG FDA UDI
GMDN Term
Patient lifting system bath chair FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5500 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: Patient lifting system bath chair

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

Similar devices

Also classified as Patient lifting system bath chair.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thermor Ltd

Sources (1)

  • FDA UDI fc74c85a-a9fe-43eb-a08f-e886ca1b5eb8 33 fields · synced May 30, 2026