RICHARDS PISTON 40MM LENGTH 4MM DIAMETER PLATINUMFLUOROPLASTIC

GUDID 00821925016804

Replace the portion of the ossicular chain that has lost its function due to disease congenital defect or other pathological process

Gyrus Acmi, Inc.

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Primary Device ID00821925016804
NIH Device Record Key2e0352b4-a065-4a80-9a79-7d0e6e9da1c1
Commercial Distribution StatusIn Commercial Distribution
Brand NameRICHARDS PISTON 40MM LENGTH 4MM DIAMETER PLATINUMFLUOROPLASTIC
Version Model Number141814
Company DUNS007198742
Company NameGyrus Acmi, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS100821925016804 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ETBProsthesis, Partial Ossicular Replacement

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

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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