Healing cap with plug 30 mm 95084

GUDID 09321502028202

N/A

Cochlear Bone Anchored Solutions AB

Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable
Primary Device ID09321502028202
NIH Device Record Key58c79a36-764f-4c6a-9fd8-bd0df00bcd7c
Commercial Distribution StatusIn Commercial Distribution
Brand NameHealing cap with plug 30 mm
Version Model Number95084
Catalog Number95084
Company DUNS559784736
Company NameCochlear Bone Anchored Solutions AB
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
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

Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com
Phone+1(800)523-5798
Emailcustomer@cochlear.com

Device Dimensions

Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter
Device Size Text, specify0
Outer Diameter30 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS109321502028202 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAHHearing aid, bone conduction, implanted

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

[09321502028202]

Radiation Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-09-14
Device Publish Date2015-11-13

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