| Primary Device ID | 10603295552345 |
| NIH Device Record Key | 1322657b-df85-46b3-90bf-37f3020c1341 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ACTIS |
| Version Model Number | 2999-66-966 |
| Catalog Number | 299966966 |
| Company DUNS | 080506581 |
| Company Name | DEPUY ORTHOPAEDICS, INC. |
| 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 | false |
| OTC Over-The-Counter | false |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10603295552345 [Primary] |
| LXH | Orthopedic manual surgical instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
[10603295552345]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-09-05 |
| Device Publish Date | 2024-08-28 |
| 10603295554974 - EMPHASYS | 2026-02-12 EMPHASYS MAKE TO ORDER CUP IMPACTOR WITH STRIKE PLATE 14.5 INCH |
| 10603295080121 - AML EXCEL | 2026-02-09 AML EXCEL FEMORAL/HUMERAL HEAD IMPACTOR |
| 10603295082408 - DURALOC | 2026-02-09 DURALOC POLY IMPACTOR HANDLE |
| 10603295083382 - SIGMA | 2026-02-09 SIGMA HP PARTIAL KNEE-UNI FEMORAL IMPACTOR |
| 10603295084075 - SIGMA | 2026-02-09 SIGMA HP PARTIAL KNEE-TROCHLEA IMPACTOR |
| 10603295088042 - GLOBAL FX | 2026-02-09 GLOBAL FX HEAD IMPACTION STAND |
| 10603295090540 - GLOBAL AP | 2026-02-09 GLOBAL AP TAPER IMPACTOR |
| 10603295090687 - GLOBAL AP | 2026-02-09 GLOBAL AP HEAD IMPACTOR |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACTIS 86386152 5023115 Live/Registered |
Johnson & Johnson 2014-09-05 |
![]() ACTIS 85294275 not registered Dead/Abandoned |
Colgate-Palmolive Company 2011-04-13 |
![]() ACTIS 85280482 not registered Dead/Abandoned |
Colgate-Palmolive Company 2011-03-29 |
![]() ACTIS 79350283 not registered Live/Pending |
Lasertec Corporation 2022-07-21 |
![]() ACTIS 79193954 5202354 Live/Registered |
Actis LLP 2016-04-13 |
![]() ACTIS 79005302 3095797 Dead/Cancelled |
Actis LLP 2004-01-30 |
![]() ACTIS 79004986 3095796 Live/Registered |
Actis LLP 2004-01-15 |
![]() ACTIS 78420722 not registered Dead/Abandoned |
STEYR-DAIMLER-PUCH SPEZIALFAHRZEUG AG &CO. KG 2004-05-18 |
![]() ACTIS 76061596 not registered Dead/Abandoned |
Actis Technology Limited 2000-06-02 |
![]() ACTIS 75821232 2542167 Live/Registered |
SIDEL PARTICIPATIONS 1999-10-12 |
![]() ACTIS 75605905 not registered Dead/Abandoned |
ACTIS, Inc. 1998-12-15 |
![]() ACTIS 75139822 2126317 Live/Registered |
VIVUS, INC. 1996-07-25 |