SHEA PORP PROSTHESIS DENSE HYDROXYLAPATITE CAP FLUOROPLASTIC SHAFT

GUDID 00821925017405

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

Gyrus Acmi, Inc.

Polyethylene craniofacial tissue reconstructive material
Primary Device ID00821925017405
NIH Device Record Keyde9112d8-7aac-4776-8447-9da5423599e8
Commercial Distribution StatusIn Commercial Distribution
Brand NameSHEA PORP PROSTHESIS DENSE HYDROXYLAPATITE CAP FLUOROPLASTIC SHAFT
Version Model Number140962
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
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Device Identifiers

Device Issuing AgencyDevice ID
GS100821925017405 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ETAReplacement, Ossicular Prosthesis, Total

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

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