G-MOPS

GUDID 07350025910819

Vitrolife Sweden AB

IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium IVF medium
Primary Device ID07350025910819
NIH Device Record Keyc3bd8a7a-b5ff-4a29-89f2-6fa33100c519
Commercial Distribution StatusIn Commercial Distribution
Brand NameG-MOPS
Version Model Number10181
Company DUNS631805488
Company NameVitrolife Sweden AB
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
GS107350025910819 [Primary]

FDA Product Code

MQLMedia, Reproductive

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-04
Device Publish Date2021-05-27

On-Brand Devices [G-MOPS]

0735002591046810129
0735002591081910181

Trademark Results [G-MOPS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
G-MOPS
G-MOPS
79355221 not registered Live/Pending
Vitrolife Sweden AB
2022-10-07

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