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Carlo Classic Alu Patient Lift

FDA UDI

Class I (US FDA UDI)

by BEKA Hospitec GmbH

Identity

Trade Name
Carlo Classic Alu Patient Lift FDA UDI
Generic Name
Mobile patient lifting system, electrically-powered FDA UDI
Device Name
Carlo Classic Alu Patient Lift FDA UDI
Model / Reference
924003218 FDA UDI
Description
Carlo Classic Alu Patient Lift FDA UDI

Identifiers

Primary DI / UDI-DI
04260735022401 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Mobile patient lifting system, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mobile patient lifting system, electrically-powered

Carlo Classic Alu Patient Lift by BEKA Hospitec GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile patient lifting system, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
BEKA Hospitec GmbH

Sources (1)

  • FDA UDI 3e39d989-74c1-4f9b-9ee9-78335024d3f0 33 fields · synced Jun 1, 2026