Primary Device ID | 03700434022735 |
NIH Device Record Key | 5ad88bd4-ebde-4a1c-8383-054b2f4fd2fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tornier Flex Shoulder System |
Version Model Number | DWF501 |
Catalog Number | DWF501 |
Company DUNS | 260324876 |
Company Name | TORNIER |
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 | true |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com | |
Phone | +330476613500 |
order@tornier.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700434022735 [Primary] |
KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-04-04 |
Device Publish Date | 2022-03-25 |