WEHRS II INCUSSTAPES PROSTHESIS DOUBLE NOTCH MEDIUM OAL 73 MM FL 61 MM HA FENE

GUDID 00821925020337

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 ID00821925020337
NIH Device Record Key5e9c4bc0-5109-438f-9306-f172c73ba89c
Commercial Distribution StatusIn Commercial Distribution
Brand NameWEHRS II INCUSSTAPES PROSTHESIS DOUBLE NOTCH MEDIUM OAL 73 MM FL 61 MM HA FENE
Version Model Number70140988
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
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Phone1(800)262-3540
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Phone1(800)262-3540
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Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
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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
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Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
Emailxxx@xxx.xxx
Phone1(800)262-3540
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Phone1(800)262-3540
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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
GS100821925020337 [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

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