Primary Device ID | 09321502021661 |
NIH Device Record Key | fca1e348-d48e-4ee4-bd1a-6a7af49b3ac0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vistafix |
Version Model Number | 92994 |
Catalog Number | 92994 |
Company DUNS | 559784736 |
Company Name | Cochlear Bone Anchored Solutions AB |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com | |
Phone | +1(800)523-5798 |
customer@cochlear.com |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 3.5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09321502021661 [Primary] |
FZE | PROSTHESIS, NOSE, INTERNAL |
Steralize Prior To Use | true |
Device Is Sterile | true |
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
[09321502021661]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-09-18 |
Device Publish Date | 2015-10-22 |
09321502021739 | Cover screw conical for Vistafix® VXI300 Implant |
09321502021722 | Cochlear™ Vistafix® VXI300 Implant 4mm |
09321502021715 | Cochlear™ Vistafix® VXI300 Implant 3mm |
09321502021708 | Cochlear™ Vistafix® VXA300 Healing abutment |
09321502021692 | Cochlear™ Vistafix® VXA300 Abutment 7.5mm |
09321502021685 | Cochlear™ Vistafix® VXA300 Abutment 6mm |
09321502021678 | Cochlear™ Vistafix® VXA300 Abutment 4.5mm |
09321502021661 | Cochlear™ Vistafix® VXA300 Abutment 3.5mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VISTAFIX 78574040 3238112 Live/Registered |
COCHLEAR BONE ANCHORED SOLUTIONS AB 2005-02-24 |