VenoTrain ulcertec

GUDID 04057532098261

Bauerfeind AG

Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use
Primary Device ID04057532098261
NIH Device Record Key2b2b2a82-49cb-41f2-b12e-cb45ad36d79a
Commercial Distribution StatusIn Commercial Distribution
Brand NameVenoTrain ulcertec
Version Model Number20960301001334
Company DUNS315914853
Company NameBauerfeind AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS104057532098261 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DWLStocking, medical support (to prevent pooling of blood in legs)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-14
Device Publish Date2020-09-04

On-Brand Devices [VenoTrain ulcertec]

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0404644587238920980000021232
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