Primary Device ID | 09321502063388 |
NIH Device Record Key | f4936af5-4295-4ccc-809a-2e4af24e29a8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Guide pin 20 mm |
Version Model Number | 90796 |
Company DUNS | 559784736 |
Company Name | Cochlear Bone Anchored Solutions AB |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
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 |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09321502063388 [Primary] |
FZE | PROSTHESIS, NOSE, INTERNAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-21 |
Device Publish Date | 2023-08-11 |
09321502016018 | Laboratory component for prior generation Vistafix |
09321502063388 | to be used to attach Impression copings to abutments and Abutment replicas when making an impres |