MCGEE WIRE CLOSING FORCEPS 3.75 MM JAW LENGTH 3.25 MM JAW LENGTH EBON

GUDID 00821925019362

Gyrus Acmi, Inc.

Rigid endoscopic grasping forceps, reusable Rigid endoscopic grasping forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable
Primary Device ID00821925019362
NIH Device Record Key0e78e1dc-458b-4ba6-8973-e752b9bfd35a
Commercial Distribution StatusIn Commercial Distribution
Brand NameMCGEE WIRE CLOSING FORCEPS 3.75 MM JAW LENGTH 3.25 MM JAW LENGTH EBON
Version Model Number230193
Company DUNS007198742
Company NameGyrus Acmi, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100821925019362 [Primary]

FDA Product Code

JXXFORCEPS, WIRE CLOSURE, ENT, STERILE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


[00821925019362]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-12
Device Publish Date2018-09-11

Devices Manufactured by Gyrus Acmi, Inc.

00810008180983 - nCare2023-10-02 nCare, D, DRCT SDI, ELA, DICOM, RCRDG
00810008180990 - nCare2023-10-02 nCare,D ,2 DRCT SDI, DICOM, RCRDG
00810008180501 - nCare2023-09-25 nCare, Sgl,Direct SDI,DICOM,Rcrdg
00810008180921 - nCare2023-09-25 nCare, Dual,ELA x 2,DICOM,Rcrdg
00810008180952 - nCare2023-09-25 nCare, SNGL,DRCT SDI,DICOM
00810008180969 - nCare2023-09-25 nCare, SNGL, ELA, DICOM
00810008180976 - nCare2023-09-25 nCare, SNGL, ELA, DICOM, RCRDG
00821925036406 - USA Elite2023-07-26 ACMI USA Elite System and USA Series Knife Electrode 24 Fr (8mm)

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