IV Administration Set

GUDID 00616784704739

DYNAREX CORPORATION

Intravenous administration set
Primary Device ID00616784704739
NIH Device Record Key21d894a3-b8fe-4a63-8d1f-775c7be23f79
Commercial Distribution Discontinuation2020-02-26
Commercial Distribution StatusNot in Commercial Distribution
Brand NameIV Administration Set
Version Model Number7047
Company DUNS008124539
Company NameDYNAREX CORPORATION
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100616784704739 [Primary]

FDA Product Code

FPASet, Administration, Intravascular

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-02-27
Device Publish Date2018-01-06

On-Brand Devices [IV Administration Set]

006167877047297047
006167847053307053
006167847052317052
006167847051327051
006167847050337050
006167847049377049
006167847048387048
006167847045247045
006167847044257044
006167847043267043
006167847039237039
006167847038247038
006167847037327037
006167847036337036
006167847035347035
006167847034357034
006167847033367033
006167847032377032
006167847031387031
006167847030397030
006167847047397047

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