Epix Laparoscopic Scissors

GUDID 10607915110120

Laparoscopic Scissors

APPLIED MEDICAL RESOURCES CORPORATION

Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
Primary Device ID10607915110120
NIH Device Record Key5c938ed9-460f-4814-9853-384e36f79cc9
Commercial Distribution StatusIn Commercial Distribution
Brand NameEpix Laparoscopic Scissors
Version Model NumberCB030
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
Length35 Centimeter
Lumen/Inner Diameter5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100607915110123 [Primary]
GS110607915110120 [Package]
Contains: 00607915110123
Package: [10 Units]
In Commercial Distribution

FDA Product Code

HETLaparoscope, Gynecologic (And Accessories)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-02-21
Device Publish Date2016-09-24

On-Brand Devices [Epix Laparoscopic Scissors]

10607915110137Laparoscopic Scissors
10607915110120Laparoscopic Scissors

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