Hasson

GUDID 00877972000563

GENICON, INC.

Laparoscopic access cannula anchor, single-use
Primary Device ID00877972000563
NIH Device Record Key48da7691-b2a5-479e-bcd1-2dbf4306805e
Commercial Distribution StatusIn Commercial Distribution
Brand NameHasson
Version Model Number400-012-131
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
GS100877972000563 [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 Number3
Public Version Date2018-07-06
Device Publish Date2017-05-05

Devices Manufactured by GENICON, INC.

00877972000334 - Kit2020-01-09
00877972000426 - GeniShield2020-01-09
00877972000433 - GeniShield2020-01-09
00877972000440 - GeniShield2020-01-09
00877972000464 - GeniShield2020-01-09
00877972000471 - GeniShield2020-01-09
00877972000488 - GeniShield2020-01-09
00877972000495 - GeniPort2020-01-09

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