Dissection Pipette

GUDID 10805360018224

VITROLIFE INC.

User-induced micropipette
Primary Device ID10805360018224
NIH Device Record Keyfcf6af9e-4b2f-43e7-8ac6-ece578da266d
Commercial Distribution StatusIn Commercial Distribution
Brand NameDissection Pipette
Version Model Number15525
Company DUNS051915038
Company NameVITROLIFE INC.
Device Count10
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
GS100805360018227 [Unit of Use]
GS110805360018224 [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 Number4
Public Version Date2020-04-21
Device Publish Date2016-09-23

On-Brand Devices [Dissection Pipette]

1080536001872915669
1080536001826215645
1080536001825515527
1080536001824815526
1080536001822415525

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