Holding Pipette

GUDID 17350025914135

Vitrolife Sweden AB

User-induced micropipette User-induced micropipette User-induced micropipette User-induced micropipette User-induced micropipette
Primary Device ID17350025914135
NIH Device Record Key0eee206a-ab88-41fc-8ec6-ea053a124d82
Commercial Distribution StatusIn Commercial Distribution
Brand NameHolding Pipette
Version Model Number14393
Company DUNS631805488
Company NameVitrolife Sweden AB
Device Count20
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
GS107350025914138 [Unit of Use]
GS117350025914135 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQHMicrotools, Assisted Reproduction (Pipettes)

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 Date2016-09-09

On-Brand Devices [Holding Pipette]

1735002591413514393
1735002591208714340
1735002591201814333
1735002591191214323
1735002591186814318
1735002591184414316
1735002591176914308

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