Follicle Aspiration Set, Reduced Single Lumen

GUDID 07350025914282

Vitrolife Sweden AB

IVF oocyte aspiration needle, single-use
Primary Device ID07350025914282
NIH Device Record Keydfb78caa-43c9-4635-9fd3-60f334ebeac0
Commercial Distribution StatusIn Commercial Distribution
Brand NameFollicle Aspiration Set, Reduced Single Lumen
Version Model Number14177
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
GS107350025914282 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQENeedle, Assisted Reproduction

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-23

On-Brand Devices [Follicle Aspiration Set, Reduced Single Lumen]

1735002591475314180
1735002591474614179
1735002591429614178
0735002591428214177
1735002591427214176
1735002591423414175

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