Silicone Tubing, Translucent

GUDID 00684995530133

16 Fr. x 100 cm

BENTEC MEDICAL OPCO, LLC

Surgical capillary wound drain, luminal, synthetic polymer
Primary Device ID00684995530133
NIH Device Record Key36287aa0-880d-4014-b7ab-02f123644b85
Commercial Distribution StatusIn Commercial Distribution
Brand NameSilicone Tubing, Translucent
Version Model NumberGS75160-16
Company DUNS080524654
Company NameBENTEC MEDICAL OPCO, LLC
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100684995530133 [Primary]

FDA Product Code

GBXCatheter, Irrigation

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-30
Device Publish Date2023-10-20

On-Brand Devices [Silicone Tubing, Translucent]

0068499553020128 Fr. x 100 cm
0068499553019526 Fr. x 100 cm
0068499553018824 Fr. x 100 cm
0068499553017122 Fr. x 100 cm
0068499553016420 Fr. x 100 cm
0068499553015719 Fr. x 100 cm
0068499553014018 Fr. x 100 cm
0068499553013316 Fr. x 100 cm
0068499553012615 Fr. x 100 cm
0068499553011914 Fr. x 100 cm
0068499553010212 Fr. x 100 cm
0068499553008910 Fr. x 100 cm
006849955300729 Fr. x 100 cm
006849955300658 Fr. x 100 cm
006849955300587 Fr. x 100 cm
006849955300416 Fr. x 100 cm
006849955300345 Fr. x 100 cm
006849955300274 Fr. x 100 cm
006849955300103 Fr. x 100 cm

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