Holding Pipette

GUDID 10805360017203

VITROLIFE INC.

User-induced micropipette
Primary Device ID10805360017203
NIH Device Record Keyc4ba01da-b814-4590-8372-3c3ef84da7e6
Commercial Distribution StatusIn Commercial Distribution
Brand NameHolding Pipette
Version Model Number15318
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
GS100805360017206 [Unit of Use]
GS110805360017203 [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 [Holding Pipette]

1080536001897215320
1080536001892715304
1080536001735715336
1080536001732615335
1080536001731915334
1080536001729615333
1080536001727215331
1080536001726515328
1080536001724115327
1080536001723415324
1080536001722715319
1080536001721015321
1080536001720315318
1080536001719715317
1080536001718015316
1080536001717315311
1080536001716615309
1080536001714215308
1080536001713515322
1080536001712815306
1080536001711115305
1080536001710415301
1080536001709815610
1080536001708115285
1080536001707415284

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