titan
GUDID 00818614021652
Beath Pin 2.4mm x 240mm
VALERIS MEDICAL LLC
Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide Orthopaedic reamer guide| Primary Device ID | 00818614021652 |
| NIH Device Record Key | 5bb45618-846f-4dc3-9329-81c8794d68fa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | titan |
| Version Model Number | 00-24GP-240 |
| Company DUNS | 079444554 |
| Company Name | VALERIS MEDICAL LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| 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 |
Device Dimensions
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
| Outer Diameter | 2.4 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00818614021652 [Primary] |
FDA Product Code
| LXI | Guide, Drill, Ligament |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
[00818614021652]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-12-28 |
| Device Publish Date | 2020-12-18 |
On-Brand Devices [titan]
| 00818614021287 | TS-5515-TI |
| 00818614021270 | TS-5015-TI |
| 00818614021263 | TS-4515-TI |
| 00818614020488 | TS-8012 |
| 00818614020471 | TS-7012 |
| 00818614020464 | TS-7015 |
| 00818614020457 | TS-6515 |
| 00818614020440 | TS-6015 |
| 00818614020433 | TS-5515 |
| 00818614020426 | TS-5015 |
| 00818614020419 | TS-4515 |
| 00818614020402 | IS-1230-TI |
| 00818614020396 | IS-1223-TI |
| 00818614020389 | IS-1130-TI |
| 00818614020372 | IS-1123-TI |
| 00818614020365 | IS-1030-TI |
| 00818614020358 | IS-1023-TI |
| 00818614020341 | IS-0930-TI |
| 00818614020334 | IS-0923-TI |
| 00818614020327 | IS-0830-TI |
| 00818614020310 | IS-0823-TI |
| 00818614020303 | IS-0730-TI |
| 00818614020297 | IS-0723-TI |
| 00818614020280 | IS-1230 |
| 00818614020273 | IS-1223 |
| 00818614020266 | IS-1130 |
| 00818614020259 | IS-1123 |
| 00818614020242 | IS-1030 |
| 00818614020235 | IS-1023 |
| 00818614020228 | IS-0930 |
| 00818614020211 | IS-0923 |
| 00818614020204 | IS-0830 |
| 00818614020198 | IS-0823 |
| 00818614020181 | IS-0730 |
| 00818614020174 | IS-0723 |
| BO48IS07230 | Titan Interference Screw, PEEK, 7 x 23mm |
| B048TS80120 | Titan Mini Interference Screw, PEEK, 8.0 x 12mm |
| B048TS70150 | Titan Mini Interference Screw, PEEK, 7.0 x 15mm |
| B048TS70120 | Titan Mini Interference Screw, PEEK, 7.0 x 12mm |
| B048TS65150 | Titan Mini Interference Screw, PEEK, 6.5 x 15mm |
| B048TS60150 | Titan Mini Interference Screw, PEEK, 6.0 x 15mm |
| B048TS55150 | Titan Mini Interference Screw, PEEK, 5.5 x 15mm |
| B048TS50150 | Titan Mini Interference Screw, PEEK, 5.0 x 15mm |
| B048TS45150 | Titan Mini Interference Screw, PEEK, 4.5 x 15mm |
| B048IS1230TI0 | Titan Interference Screw, Titanium, 12 x 30mm |
| B048IS12300 | Titan Interference Screw, PEEK, 12 x 30mm |
| B048IS1223TI0 | Titan Interference Screw, Titanium, 12 x 23mm |
| B048IS12230 | Titan Interference Screw, PEEK, 12 x 23mm |
| B048IS1130TI0 | Titan Interference Screw, Titanium, 11 x 30mm |
| B048IS11300 | Titan Interference Screw, PEEK, 11 x 30mm |
Trademark Results [titan]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TITAN 98516875 not registered Live/Pending |
Accela Group LLC 2024-04-24 |
 TITAN 98516811 not registered Live/Pending |
Accela Group LLC 2024-04-24 |
 TITAN 98431869 not registered Live/Pending |
Masonry Support Systems Limited 2024-03-04 |
 TITAN 98429630 not registered Live/Pending |
Titan Cement Company S.A. 2024-03-01 |
 TITAN 98377409 not registered Live/Pending |
Custom Packaging & Products, Inc. 2024-01-26 |
 TITAN 98371871 not registered Live/Pending |
Winpak Lane, Inc. 2024-01-23 |
 TITAN 98305557 not registered Live/Pending |
Titan Wheel Accessories LLC 2023-12-08 |
 TITAN 98297749 not registered Live/Pending |
Langmuir Systems LLC 2023-12-04 |
 TITAN 98251992 not registered Live/Pending |
THE CHALLENGE MACHINERY COMPANY 2023-11-02 |
 TITAN 98246264 not registered Live/Pending |
Creative Plastic Concepts, LLC 2023-10-30 |
 TITAN 98246134 not registered Live/Pending |
Creative Plastic Concepts, LLC 2023-10-30 |
 TITAN 98246117 not registered Live/Pending |
Creative Plastic Concepts, LLC 2023-10-30 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.