Nora Pro Stand Aid

GUDID 04260681890222

Stand Aid

BEKA Hospitec GmbH

General-purpose patient lifting system sling/harness
Primary Device ID04260681890222
NIH Device Record Keyf8e127e1-851a-400e-8fb9-8d93da960528
Commercial Distribution StatusIn Commercial Distribution
Brand NameNora Pro Stand Aid
Version Model Number921078000
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
GS104260681890222 [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 [Nora Pro Stand Aid ]

04260735020407Stand Aid
04260681890222Stand Aid

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.