Kii Optical Access System

GUDID 10607915140172

Trocar

APPLIED MEDICAL RESOURCES CORPORATION

Laparoscopic access cannula, single-use Laparoscopic access cannula, single-use
Primary Device ID10607915140172
NIH Device Record Key0a111490-acaf-42fd-9265-92c310da37ac
Commercial Distribution StatusIn Commercial Distribution
Brand NameKii Optical Access System
Version Model NumberCFR39
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

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

Device Dimensions

Length150 Millimeter
Lumen/Inner Diameter15 Millimeter
Length150 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100607915140175 [Primary]
GS110607915140172 [Package]
Contains: 00607915140175
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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-28
Device Publish Date2020-01-20

On-Brand Devices [Kii Optical Access System]

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10607915123038Trocar
10607915122291Trocar
10607915119956Trocar
10607915119895Trocar
10607915119888Trocar
10607915140172Trocar

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