Primary Device ID | 08033390084390 |
NIH Device Record Key | efdbae37-d9ff-4902-a2b7-14dc3b53d718 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TT MB Peg |
Version Model Number | TT Glenoid |
Catalog Number | 1375.14.652 |
Company DUNS | 432066322 |
Company Name | LIMACORPORATE SPA |
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 | 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 |
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 | 08033390084390 [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 | 2015-08-04 |
08033390084406 | SMR TT Metal Back Peg (Ti6Al4V) - S-R Long |
08033390084390 | SMR TT Metal Back Peg (Ti6Al4V) - S-R Medium |