Hatching Pipette

GUDID 10805360016091

VITROLIFE INC.

User-induced micropipette
Primary Device ID10805360016091
NIH Device Record Key06f259ad-7ef4-4dff-98d2-389b408689c8
Commercial Distribution StatusIn Commercial Distribution
Brand NameHatching Pipette
Version Model Number15104
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
GS100805360016094 [Unit of Use]
GS110805360016091 [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 [Hatching Pipette]

1080536001889715140
1080536001887315139
1080536001873615670
1080536001715915141
1080536001619015111
1080536001618315110
1080536001616915109
1080536001613815108
1080536001612115107
1080536001611415106
1080536001610715105
1080536001609115104
1080536001607715103
1080536001606015102
1080536001605315130

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