HeadPiece Small

GUDID 07630016805769

Beige

Advanced Bionics AG

Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant system coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil Cochlear implant/auditory brainstem implant coil
Primary Device ID07630016805769
NIH Device Record Key70c5898d-1cde-49f2-834d-a928b5c34d68
Commercial Distribution StatusIn Commercial Distribution
Brand NameHeadPiece Small
Version Model NumberMMT-5300-00
Company DUNS485262658
Company NameAdvanced Bionics AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx
Phone+1(661)362-1400
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS107630016805769 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MCMIMPLANT, COCHLEAR

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-05

On-Brand Devices [HeadPiece Small]

07630016805776Brown
07630016805769Beige

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