Primary Device ID | 00856037005798 |
NIH Device Record Key | b1e2f833-f132-49e2-ae44-a45e13579d95 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TiLink-P |
Version Model Number | PPT-P2611010-S |
Catalog Number | PPT-P2611010-S |
Company DUNS | 010968002 |
Company Name | Tyber Medical LLC |
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 |
Phone | +1(866)761-0933 |
jstigliano@tybermed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00856037005798 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2019-11-13 |
00856037005156 | TiLink-P 26mm x 10mm x 15mm x 8 deg |
00856037005149 | TiLink-P 26mm x 10mm x 13mm x 8 deg |
00856037005132 | TiLink-P 26mm x 10mm x 12mm x 8 deg |
00856037005101 | TiLink-P 26mm x 10mm x 9mm x 8 deg |
00856037005095 | TiLink-P 26mm x 10mm x 8mm x 8 deg |
00856037005088 | TiLink-P 26mm x 10mm x 7mm x 8 deg |
00856037005828 | TiLink-P - 26mm x 10mm x 9mm x 0° |
00856037005811 | TiLink-P - 26mm x 10mm x 8mm x 0° |
00856037005804 | TiLink-P - 26mm x 10mm x 12mm x 0° |
00856037005798 | TiLink-P - 26mm x 10mm x 11mm x 0° |
00856037005781 | TiLink-P - 26mm x 10mm x 10mm x 0° |