Kii® Shielded Bladed Access System

GUDID 10607915116528

Trocars

APPLIED MEDICAL RESOURCES CORPORATION

Laparoscopic access cannula, single-use
Primary Device ID10607915116528
NIH Device Record Key6cd86870-ff14-4936-a4f5-b21ead754ea1
Commercial Distribution StatusIn Commercial Distribution
Brand NameKii® Shielded Bladed Access System
Version Model NumberC0R67
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
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
Phone1.949.713.8300
Emailcontact@appliedmedical.com
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 Diameter12 Millimeter
Lumen/Inner Diameter12 Millimeter
Lumen/Inner Diameter12 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter
Length100 Millimeter
Lumen/Inner Diameter12 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100607915116521 [Primary]
GS110607915116528 [Package]
Contains: 00607915116521
Package: [6 Units]
Discontinued: 2016-08-17
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 Date2016-08-17

On-Brand Devices [Kii® Shielded Bladed Access System]

10607915116542Trocars
10607915116528Trocars
10607915116481Trocars
10607915116474Trocars

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