Silicone Penrose Straight Drain Tube

GUDID 04710961934752

FORTUNE MEDICAL INSTRUMENT CORP.

Surgical capillary wound drain, luminal, synthetic polymer
Primary Device ID04710961934752
NIH Device Record Key1f071276-759a-4b2a-815d-bd8974eba3bc
Commercial Distribution StatusIn Commercial Distribution
Brand NameSilicone Penrose Straight Drain Tube
Version Model Number2011-0020
Company DUNS656763489
Company NameFORTUNE MEDICAL INSTRUMENT CORP.
Device Count10
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 Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104710961934752 [Unit of Use]
GS114710961934759 [Primary]

FDA Product Code

GBPCatheter, Multiple Lumen

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-11-30
Device Publish Date2021-11-22

On-Brand Devices [Silicone Penrose Straight Drain Tube]

047109619347522011-0020
047109619347832011-0045
047109619347762011-0035
047109619347692011-0025

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