Guide pin 20 mm 90796

GUDID 09321502016018

Laboratory component for prior generation Vistafix

Cochlear Bone Anchored Solutions AB

General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use General external orthopaedic fixation system implantation kit, single-use
Primary Device ID09321502016018
NIH Device Record Key334f8ca9-e5e1-4d98-88e5-164a879980f1
Commercial Distribution StatusIn Commercial Distribution
Brand NameGuide pin 20 mm
Version Model Number90796
Catalog Number90796
Company DUNS559784736
Company NameCochlear Bone Anchored Solutions AB
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
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

Device Dimensions

Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
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Length20 Millimeter
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Length20 Millimeter
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Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter
Device Size Text, specify0
Length20 Millimeter

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store at room temperature

Device Identifiers

Device Issuing AgencyDevice ID
GS109321502016018 [Primary]

FDA Product Code

FZEPROSTHESIS, NOSE, INTERNAL

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-12-17
Device Publish Date2017-06-07

On-Brand Devices [Guide pin 20 mm]

09321502016018Laboratory component for prior generation Vistafix
09321502063388to be used to attach Impression copings to abutments and Abutment replicas when making an impres

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