Silicone Tubing, Penrose Drain

GUDID 10684995520025

1/2 in. x 12 in. Length

BENTEC MEDICAL OPCO, LLC

Surgical capillary wound drain, luminal, synthetic polymer
Primary Device ID10684995520025
NIH Device Record Key21158135-4aa2-40e8-b83d-fd72fe0d7c8e
Commercial Distribution StatusIn Commercial Distribution
Brand NameSilicone Tubing, Penrose Drain
Version Model NumberGR103
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
GS100684995520028 [Primary]
GS110684995520025 [Package]
Contains: 00684995520028
Package: [25 Units]
In Commercial Distribution

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, Penrose Drain]

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106849955201171 in. x 18 in. Length
106849955201003/4 in. x 18 in. Length
106849955200945/8 in. x 18 in. Length
106849955200871/2 in. x 18 in. Length
106849955200703/8 in. x 18 in. Length
106849955200631/4 in. x 18 in. Length
106849955200561 in. x 12 in. Length
106849955200493/4 in. x 12 in. Length
106849955200325/8 in. x 12 in. Length
106849955200251/2 in. x 12 in. Length
106849955200183/8 in. x 12 in. Length
106849955200011/4 in. x 12 in. Length

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