Kii Optical Access System

GUDID 10607915119956

Trocar

APPLIED MEDICAL RESOURCES CORPORATION

Laparoscopic access cannula, single-use Laparoscopic access cannula, single-use Laparoscopic access cannula, single-use
Primary Device ID10607915119956
NIH Device Record Key48fe1e64-6246-4e9d-a7e6-32105bb9de4f
Commercial Distribution StatusIn Commercial Distribution
Brand NameKii Optical Access System
Version Model NumberCFR31
Company DUNS187129135
Company NameAPPLIED MEDICAL RESOURCES CORPORATION
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com

Device Dimensions

Lumen/Inner Diameter11 Millimeter
Lumen/Inner Diameter11 Millimeter
Lumen/Inner Diameter11 Millimeter
Lumen/Inner Diameter11 Millimeter
Length150 Millimeter
Lumen/Inner Diameter11 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100607915119959 [Primary]
GS110607915119956 [Package]
Contains: 00607915119959
Package: [6 Units]
In Commercial Distribution

FDA Product Code

GCJLaparoscope, 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 Date2020-01-09
Device Publish Date2016-09-13

On-Brand Devices [Kii Optical Access System]

10607915125742Trocar
10607915125735Trocar
10607915123229Trocar
10607915123038Trocar
10607915122291Trocar
10607915119956Trocar
10607915119895Trocar
10607915119888Trocar
10607915140172Trocar

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