Primary Device ID | 18054242512356 |
NIH Device Record Key | 655c5756-7b0d-4fb5-9bc2-2e3a2d3131c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | True Lok System |
Version Model Number | 1 |
Catalog Number | 99-56-20220 |
Company DUNS | 438793622 |
Company Name | ORTHOFIX SRL |
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 | true |
Manufacturing Date | true |
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 | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it | |
Phone | +039456719000 |
info@orthofix.it |
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 | 18054242512356 [Primary] |
OSN | Software For Diagnosis/Treatment |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-09-01 |
18054242513100 | TRUE LOK TRAUMA U-SUPPORT, 200MM STERILE |
18054242512752 | K-WIRE, 550MM, OLIVE TL-HEX STERILE |
18054242512745 | K-WIRE, 450MM, NO OLIVE TL-HEX STERILE |
18054242512639 | DOUBLE ROW FOOTPLATE, 220MM, TL-HEX STERILE |
18054242512622 | DOUBLE ROW FOOTPLATE, 200MM, TL-HEX STERILE |
18054242512615 | DOUBLE ROW FOOTPLATE, 180MM, TL-HEX STERILE |
18054242512608 | DOUBLE ROW FOOTPLATE, 160MM, TL-HEX STERILE |
18054242512592 | DOUBLE ROW FOOTPLATE, 140MM, TL-HEX STERILE |
18054242512585 | DOUBLE ROW FOOTPLATE, 120MM, TL-HEX STERILE |
18054242512578 | 3/8 RING, 300MM, TL-HEX STERILE |
18054242512561 | 3/8 RING, 280MM, TL-HEX STERILE |
18054242512554 | 3/8 RING, 240MM, TL-HEX STERILE |
18054242512547 | 3/8 RING, 220MM, TL-HEX STERILE |
18054242512479 | MODULAR 5/8 RING, 300MM TL-HEX STERILE |
18054242512462 | MODULAR 5/8 RING, 280MM TL-HEX STERILE |
18054242512455 | MODULAR 5/8 RING, 240MM TL-HEX STERILE |
18054242512448 | MODULAR 5/8 RING, 220MM TL-HEX STERILE |
18054242512370 | FULL RING, 300MM, TL-HEX STERILE |
18054242512363 | FULL RING, 280MM, TL-HEX STERILE |
18054242512356 | FULL RING, 240MM, TL-HEX STERILE |
18054242511847 | TL-HEX APPLICATION SOFTWARE |
18054242510772 | 5/8 RING, 220MM, TL-HEX STERILE |
18054242510727 | FULL RING, 220MM, TL-HEX STERILE |