Carlo Alu Comfort EP Patient Lift

GUDID 04260735022432

Carlo Alu Comfort EP Patient Lift

BEKA Hospitec GmbH

Mobile patient lifting system, electrically-powered
Primary Device ID04260735022432
NIH Device Record Key1ae9bc38-321f-4155-aedd-8cca64c6913f
Commercial Distribution StatusIn Commercial Distribution
Brand NameCarlo Alu Comfort EP Patient Lift
Version Model Number925006018
Company DUNS342212273
Company NameBEKA Hospitec GmbH
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS104260735022432 [Primary]

FDA Product Code

FSALift, Patient, Non-Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-04-08
Device Publish Date2025-03-31

On-Brand Devices [Carlo Alu Comfort EP Patient Lift]

04260735022432Carlo Alu Comfort EP Patient Lift
04260735020872Carlo Alu Comfort EP Patient Lift
04260735020865Carlo Alu Comfort EP Patient Lift
04260735020759Carlo Alu Comfort EP Patient Lift
04260735020742Carlo Alu Comfort EP Patient Lift

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