Vial Adapter MEDIC'UP 1MVA0004/1

GUDID 03701225770149

Sterile Medical Device. Use for the transfer and mixing of drugs contained in vials.

UNION PLASTIC

Medication transfer set
Primary Device ID03701225770149
NIH Device Record Key8129fa0c-14ca-4f8f-be42-6183bd20774f
Commercial Distribution StatusIn Commercial Distribution
Brand NameVial Adapter MEDIC'UP
Version Model NumberØ13mm without filter
Catalog Number1MVA0004/1
Company DUNS381128396
Company NameUNION PLASTIC
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
GS103701225770149 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LHISet, I.V. Fluid Transfer

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


[03701225770149]

Radiation Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-05
Device Publish Date2024-06-27