Primary Device ID | 00846832094776 |
NIH Device Record Key | f611cef5-b88d-4639-94aa-a728913eb331 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aequalis Flex Revive |
Version Model Number | ARS744106 |
Catalog Number | ARS744106 |
Company DUNS | 968990812 |
Company Name | TORNIER, INC. |
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(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Outer Diameter | 19 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00846832094776 [Primary] |
HSD | PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
[00846832094776]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-23 |
Device Publish Date | 2022-11-15 |
00846832094783 | Trial Proximal Body Screw |
00846832094776 | Screwless Trial Proximal Body |
00846832094769 | Screwless Trial Proximal Body |
00846832094752 | Screwless Trial Proximal Body |
00846832094745 | Screwless Trial Proximal Body |
00846832094738 | Screwless Trial Proximal Body |
00846832094721 | Screwless Trial Proximal Body |