Silicone Round Drain Kit

GUDID 04710961935636

FORTUNE MEDICAL INSTRUMENT CORP.

Closed-wound drain
Primary Device ID04710961935636
NIH Device Record Key308b9233-6ead-41d7-a0d9-48846fe63dc1
Commercial Distribution StatusIn Commercial Distribution
Brand NameSilicone Round Drain Kit
Version Model Number2015-9214
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
GS104710961935636 [Unit of Use]
GS114710961935633 [Primary]

FDA Product Code

GCDConnector, Catheter

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-01-17
Device Publish Date2022-01-07

On-Brand Devices [Silicone Round Drain Kit]

047111826074492015-9314
047109619357662015-9320
047109619357592015-9318
047109619357422015-9316
047109619357352015-9310
047109619357282015-9308
047109619356672015-9220
047109619356502015-9218
047109619356432015-9216
047109619356362015-9214
047109619356292015-9210
047109619356122015-9208

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