Primary Device ID | 03700386935831 |
NIH Device Record Key | 864a4c1c-f9d3-43bb-81f1-dff7ed8284ac |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AEQUALIS REVERSED II |
Version Model Number | DWD181 |
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 | false |
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 | |
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 |
Outer Diameter | 36 Millimeter |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700386935831 [Primary] |
KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-12-23 |
Device Publish Date | 2015-10-16 |