USA Elite System™ and USA Series™ Cold Knife, Serrated Blade

GUDID 00821925002678

Gyrus Acmi, Inc.

Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome Urethrotome
Primary Device ID00821925002678
NIH Device Record Keyf18be898-e558-4613-89ee-43363af725a3
Commercial Distribution StatusIn Commercial Distribution
Brand NameUSA Elite System™ and USA Series™ Cold Knife, Serrated Blade
Version Model NumberK-SE
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 Usetrue
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
GS100821925002678 [Package]
Contains: 00821925038417
Package: [3 Units]
In Commercial Distribution
GS100821925038417 [Primary]

FDA Product Code

EZOUrethrotome

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-10-14

Devices Manufactured by Gyrus Acmi, Inc.

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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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