| Primary Device ID | 00885554024135 | 
| NIH Device Record Key | a467c6c6-3665-43fd-aaf5-56164f6186e3 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Version Model Number | 72203203 | 
| Catalog Number | 72203203 | 
| Company DUNS | 045483575 | 
| Company Name | Smith & Nephew, Inc. | 
| 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 | false | 
| Lot Batch | false | 
| Serial Number | true | 
| 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)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 | 
| GUDID@SMITH-NEPHEW.COM | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00885554024135 [Primary] | 
| OLO | Orthopedic stereotaxic instrument | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2023-09-07 | 
| Device Publish Date | 2022-12-14 | 
| 00885556909393 - NA | 2025-10-02 Cup Impactor - Offset | 
| 00885556906941 - EVOS | 2025-10-01 EVOS PELVIC 3.5MM LOCKING CURVED RECON PLATE 10 HOLE | 
| 00885556907207 - EVOS | 2025-10-01 EVOS PELVIC 2.7MM SHORT SEGMENT CURVED UTILITY PLATE | 
| 00885556907214 - EVOS | 2025-10-01 EVOS PELVIC 2.7/3.5MM SHORT SEGMENT CURVED UTILITY PLATE 2 HOLE | 
| 00885556907221 - EVOS | 2025-10-01 EVOS PELVIC 2.7/3.5MM SHORT SEGMENT CURVED UTILITY PLATE 4 HOLE | 
| 00885556907245 - EVOS | 2025-10-01 EVOS PELVIC 3.5MM SYMPHYSIS NON-LOCKING PLATE STANDARD 6 HOLE | 
| 00885556907252 - EVOS | 2025-10-01 EVOS PELVIC 3.5MM SYMPHYSIS NON-LOCKING PLATE STANDARD 8 HOLE | 
| 00885556907290 - EVOS | 2025-10-01 EVOS PELVIC 2.7MM/3.5MM SYMPHYSIS LOCKING PLATE TABBED 4 HOLE |