| Primary Device ID | 03596010470379 |
| NIH Device Record Key | 64b0035a-ec11-43e4-b897-782ca656aabf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ABLATOR |
| Version Model Number | 7209655 |
| Catalog Number | 7209655 |
| 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 | 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 | |
| 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 | 03596010470379 [Primary] |
| HRX | ARTHROSCOPE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2023-09-07 |
| Device Publish Date | 2015-08-30 |
| 03596010470423 | CHISEL VULCAN STRAIGHT W/INTEGRATED CBL |
| 03596010470393 | ABLATOR-S VULCAN 60 DEG |
| 03596010470355 | ABLATOR VULCAN 60 DEG |
| 03596010470584 | ABLATOR-S MICRO VULCAN 2MM 60 DEG |
| 03596010470577 | ABLATOR VULCAN 60 DEG 2.0MM |
| 03596010470416 | ABLATOR-S VULCAN 90 DEG HP |
| 03596010470409 | ABLATOR-S 2MM 60DEG |
| 03596010470386 | ABLATOR-S VULCAN 90 DEG |
| 03596010470379 | ABLATOR VULCAN 90 DEG HP |
| 03596010470362 | ABLATOR MICRO VULCAN INTEGRATED |
| 03596010470348 | PROBE ABLATOR 30 DEG |
| 03596010470331 | VULCAN ABLATOR 90 DEG INTEGRATED |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ABLATOR 75820958 2585958 Live/Registered |
Oratec Interventions, Inc. 1999-10-12 |