VenoTrain soft S

GUDID 04057532408244

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 Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use
Primary Device ID04057532408244
NIH Device Record Key2f7a1b9d-01a6-42b7-9ba4-bc97278b5e9f
Commercial Distribution StatusIn Commercial Distribution
Brand NameVenoTrain soft S
Version Model Number21264511504224
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
GS104057532408244 [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 Date2021-10-08
Device Publish Date2021-09-30

On-Brand Devices [VenoTrain soft S]

0405753218703321260521224334
0405753218702621260521224333
0405753218701921260521224332
0405753218700221260521224331
0405753218699921260521224324
0405753218698221260521224323
0405753218697521260521224322
0405753218696821260521224321
0405753218695121260521224234
0405753218694421260521224233
0405753218693721260521224232
0405753218692021260521224231
0405753218691321260521224224
0405753218690621260521224223
0405753218689021260521224222
0405753218688321260521224221
0405753218672221260521204334
0405753218671521260521204333
0405753218670821260521204332
0405753218669221260521204331
0405753218668521260521204324
0405753218667821260521204323
0405753218666121260521204322
0405753218665421260521204321
0405753218664721260521204234
0405753218663021260521204233
0405753218662321260521204232
0405753218661621260521204231
0405753218660921260521204224
0405753218659321260521204223
0405753218658621260521204222
0405753218657921260521204221
0405753218451321260511224334
0405753218450621260511224333
0405753218449021260511224332
0405753218448321260511224331
0405753218447621260511224324
0405753218446921260511224323
0405753218445221260511224322
0405753218444521260511224321
0405753218443821260511224234
0405753218442121260511224233
0405753218441421260511224232
0405753218440721260511224231
0405753218439121260511224224
0405753218438421260511224223
0405753218437721260511224222
0405753218436021260511224221
0405753218419321260511204334
0405753218418621260511204333

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.