| Primary Device ID | 00885556894569 |
| NIH Device Record Key | 71ae3dac-6cc0-4f17-9962-65db801f4c8f |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 72700580 |
| Catalog Number | 72700580 |
| Company DUNS | 045483575 |
| Company Name | Smith & Nephew, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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(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 | |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Special Storage Condition, Specify | Between 0 and 0 *: - |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885556894569 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-16 |
| Device Publish Date | 2025-05-08 |
| 00885556897102 - INTERTAN MAX | 2025-11-19 INTERTAN MAX 10MM X 24CM X 125D LEFT |
| 00885556897119 - INTERTAN MAX | 2025-11-19 INTERTAN MAX 10MM X 24CM X 125D RIGHT |
| 00885556897126 - INTERTAN MAX | 2025-11-19 INTERTAN MAX 11.5MM X 24CM X 125D LEFT |
| 00885556897133 - INTERTAN MAX | 2025-11-19 INTERTAN MAX 11.5MM X 24CM X 125D RIGHT |
| 00885556897201 - INTERTAN MAX | 2025-11-19 INTERTAN MAX 9MM X 38CM X 125D LEFT |
| 00885556897218 - INTERTAN MAX | 2025-11-19 INTERTAN MAX 9MM X 40CM X 125D LEFT |
| 00885556897225 - INTERTAN MAX | 2025-11-19 INTERTAN MAX 9MM X 42CM X 125D LEFT |
| 00885556897232 - INTERTAN MAX | 2025-11-19 INTERTAN MAX 9MM X 44CM X 125D LEFT |