BAROVAC® Evacuator Closed Wound Drainage System(PP)

GUDID 08806369456104

BAROVAC PP 400-4.8

Sewoon Medical Co., Ltd.

Closed-wound drainage kit
Primary Device ID08806369456104
NIH Device Record Key4d235654-7a32-4f37-aff3-3ccb208bbd1e
Commercial Distribution StatusIn Commercial Distribution
Brand NameBAROVAC® Evacuator Closed Wound Drainage System(PP)
Version Model NumberPP400L(4.8)N2
Company DUNS687784405
Company NameSewoon Medical Co., Ltd.
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108806369456104 [Primary]

FDA Product Code

GCYApparatus, Suction, Single Patient Use, Portable, Nonpowered

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-03
Device Publish Date2023-07-26

On-Brand Devices [BAROVAC® Evacuator Closed Wound Drainage System(PP)]

08806369498722BAROVAC PP 400-3.2
08806369498708BAROVAC PP 200-4.8
08806369456500BAROVAC PP 800-4.8
08806369456104BAROVAC PP 400-4.8
08806369456081BAROVAC PP 400-3.2
08806369456043BAROVAC PP 400-4.8
08806369456029BAROVAC PP 400-3.2
08806369455503BAROVAC PP 200-3.2
08806369427777PP400L(4.8)S
08806369427739PP400M(3.2)S
08806369427692BAROVAC PP 400-2.4
08806369427654PP400L(4.8)N273
08806369427616BAROVAC PP 400-3.2

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