Kii® Sheilded Bladed Dual Pack

GUDID 10607915116092

Trocars

APPLIED MEDICAL RESOURCES CORPORATION

Laparoscopic access cannula, single-use
Primary Device ID10607915116092
NIH Device Record Key4253020a-ee7c-41dc-b723-5071b7584fe6
Commercial Distribution Discontinuation2016-08-16
Commercial Distribution StatusNot in Commercial Distribution
Brand NameKii® Sheilded Bladed Dual Pack
Version Model NumberC0Q56
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
Phone1.949.713.8300
Emailcontact@appliedmedical.com

Device Dimensions

Lumen/Inner Diameter5 Millimeter
Lumen/Inner Diameter5 Millimeter
Lumen/Inner Diameter5 Millimeter
Lumen/Inner Diameter5 Millimeter
Length150 Millimeter
Lumen/Inner Diameter5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100607915116095 [Primary]
GS110607915116092 [Package]
Contains: 00607915116095
Package: [10 Units]
Discontinued: 2016-08-16
Not 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 Number4
Public Version Date2020-01-29
Device Publish Date2016-08-16

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