| Primary Device ID | 14063108105629 |
| NIH Device Record Key | 253ef354-c77b-4470-98a9-73ff1a3d51c5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TONN™ NOVATECH® |
| Version Model Number | 02BRSR133 |
| Catalog Number | 02BRSR133 |
| Company DUNS | 777211640 |
| Company Name | NOVATECH |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 14063108105629 [Primary] |
| LRC | Instrument, Ent Manual Surgical |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
[14063108105629]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-20 |
| Device Publish Date | 2023-06-12 |
| 14063108105704 | Folding Device, white |
| 14063108105698 | Loading Rod, white |
| 14063108105681 | Pusher, white |
| 14063108105674 | lntroducer Tube, white |
| 14063108105667 | Stent Applicator, white |
| 14063108105650 | Clamping Rod, red |
| 14063108105643 | Basic Block, red |
| 14063108105636 | Folding Device, red |
| 14063108105629 | Loading Rod, red |
| 14063108105612 | Pusher, red |
| 14063108105605 | Introducer Tube, red |
| 14063108105599 | Stent Applicator, red |
| 14063108105582 | Folding Device, green |
| 14063108105575 | Loading Rod, green |
| 14063108105568 | Pusher, green |
| 14063108105551 | Introducer Tube, green |
| 14063108105544 | Stent Applicator, green |
| 14063108105537 | Clamping Rod, blue/green/white |
| 14063108105520 | Basic Block, blue/green/white |
| 14063108105513 | Folding Device, blue |
| 14063108105506 | Loading Rod, blue |
| 14063108105490 | Pusher, blue |
| 14063108105483 | Introducer Tube, blue |
| 14063108105476 | Stent Applicator, blue |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TONN 76274789 not registered Dead/Abandoned |
Cape Fear River Wood Corporation, The 2001-06-21 |