VacLok AT™ VAC220/A

GUDID 20884450610712

Merit Medical Systems, Inc.

General-purpose syringe, single-use
Primary Device ID20884450610712
NIH Device Record Key4d7bd632-7cba-420b-8339-5d63f10ec7b9
Commercial Distribution StatusIn Commercial Distribution
Brand NameVacLok AT™
Version Model Number00884450610718
Catalog NumberVAC220/A
Company DUNS184763290
Company NameMerit Medical Systems, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100884450610718 [Primary]
GS110884450610715 [Package]
Contains: 00884450610718
Package: [20 Units]
In Commercial Distribution
GS120884450610712 [Package]
Contains: 10884450610715
Package: [4 Units]
In Commercial Distribution

FDA Product Code

PURVacuum syringe

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-15
Device Publish Date2022-08-06

On-Brand Devices [VacLok AT™]

2088445027179100884450271797
1088445027178700884450271780
2088445061071200884450610718
1088445061072200884450610725

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