Biopsy Pipette

GUDID 10805360016312

VITROLIFE INC.

User-induced micropipette
Primary Device ID10805360016312
NIH Device Record Key051edd4c-c3a8-49ba-b7b9-647649a76d67
Commercial Distribution StatusIn Commercial Distribution
Brand NameBiopsy Pipette
Version Model Number15120
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
GS100805360016315 [Unit of Use]
GS110805360016312 [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 [Biopsy Pipette]

1080536001886615138
1080536001863715660
1080536001759315142
1080536001705015133
1080536001686215152
1080536001653415151
1080536001652715150
1080536001651015149
1080536001648015148
1080536001647315147
1080536001646615146
1080536001643515144
1080536001642815129
1080536001641115604
1080536001640415128
1080536001639815127
1080536001638115126
1080536001637415125
1080536001636715124
1080536001635015123
1080536001634315603
1080536001633615122
1080536001632915121
1080536001631215120
1080536001630515119
1080536001629915118
1080536001628215117
1080536001627515116
1080536001626815143
1080536001625115115
1080536001624415114
1080536001623715113
1080536001622015602
1080536001621315112
1080536001620615646
1080536001614515605
1080536001602215601
0080536001644515145

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