Kii® Sheilded Bladed Access Sysem

GUDID 10607915116023

Trocars

APPLIED MEDICAL RESOURCES CORPORATION

Laparoscopic access cannula, single-use
Primary Device ID10607915116023
NIH Device Record Key6750ad1a-ead4-486f-ba25-60326de94477
Commercial Distribution StatusIn Commercial Distribution
Brand NameKii® Sheilded Bladed Access Sysem
Version Model NumberC0Q49
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
Length100 Millimeter
Lumen/Inner Diameter5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100607915116026 [Primary]
GS110607915116023 [Package]
Contains: 00607915116026
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 Date2016-08-12

On-Brand Devices [Kii® Sheilded Bladed Access Sysem]

10607915116146Trocar
10607915116139Trocars
10607915116054Trocars
10607915116047Trocars
10607915116023Trocars
10607915116016Trocars

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.