BD

GUDID 03770034301134

UNIVERDERM

Peripheral intravenous cannula
Primary Device ID03770034301134
NIH Device Record Key4f4db8c7-526f-458f-ac08-007b533c8792
Commercial Distribution StatusIn Commercial Distribution
Brand NameBD
Version Model NumberInsyte Autoguard Winged
Company DUNS281488639
Company NameUNIVERDERM
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS103770034301134 [Package]
Contains: 03770034301141
Package: [50 Units]
In Commercial Distribution
GS103770034301141 [Primary]

FDA Product Code

FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-02-07
Device Publish Date2025-01-30

Devices Manufactured by UNIVERDERM

03770034301134 - BD2025-02-07
03770034301134 - BD2025-02-07
03770034301097 - Radiesse2024-12-10
03770034301127 - Sculptra2024-12-10
03770034301110 - Restylane Eyelight 2024-12-03
03770034301004 - Juvederm2024-03-05
03770034301011 - Juvederm2024-03-05
03770034301028 - Restylane2024-03-05
03770034301035 - Restylane2024-03-05

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