GeniPort

GUDID 00877972003526

GENICON, INC.

Laparoscopic access cannula, single-use
Primary Device ID00877972003526
NIH Device Record Keya48efe3a-778a-4da0-a8e3-a5bbeb9ecc11
Commercial Distribution StatusIn Commercial Distribution
Brand NameGeniPort
Version Model Number100-105-002
Company DUNS079805400
Company NameGENICON, INC.
Device Count1
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100877972003526 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEACannula, Surgical, General & Plastic Surgery

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-01-09
Device Publish Date2017-05-05

On-Brand Devices [GeniPort]

00877972003601100-105-102
00877972003588100-105-101
00877972003526100-105-002
00877972003502100-105-001
00877972001874100-005-102
00877972001867100-005-101
00877972001850100-005-100
00877972000518100-005-002
00877972000501100-005-001
00877972000495100-005-000

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