Straumann® TL WN-compatible 9001303
GUDID 00842092181904
Straumann® TL WN-compatible Digital Analog Kit contains: 1 Straumann® TL WN-compatible Digital Analog 1 Digital Analog Base Screw
Preat Corporation
Dental implant abutment analog, scanning| Primary Device ID | 00842092181904 |
| NIH Device Record Key | ee63fc7a-0d65-47a3-a316-637c10caf78c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Straumann® TL WN-compatible |
| Version Model Number | 9001303 |
| Catalog Number | 9001303 |
| Company DUNS | 117776048 |
| Company Name | Preat Corporation |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| 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 | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com | |
| Phone | +1 (800) 232-7732 |
| info@preat.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00842092181898 [Primary] |
| GS1 | 00842092181904 [Package] Contains: 00842092181898 Package: Pack [10 Units] In Commercial Distribution |
FDA Product Code
| NDP | Accessories, Implant, Dental, Endosseous |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-14 |
| Device Publish Date | 2024-02-06 |
Devices Manufactured by Preat Corporation
| 00842092182468 - Sphero | 2024-09-02 Sphero Block Abutment Hiossen Standard x 0mm (1.8mm Ball) |
| 00842092182475 - Sphero | 2024-09-02 Sphero Block Abutment Hiossen Standard x 1mm (1.8mm Ball) |
| 00842092182444 - Equator | 2024-08-05 Equater Abutment for Astra TX 3.5/4.0 x 2mm |
| 00842092182451 - Equator | 2024-08-05 Equator Abutment for Straumann SC x 3mm |
| 00842092182277 - Equator | 2024-07-08 Equator Abutment for Astra TX 3.0 x 4mm |
| 00842092182284 - Equator | 2024-07-08 Equator Abutment for Astra TX 3.0 x 5mm |
| 00842092182291 - Equator | 2024-07-08 Equator Abutment for Astra TX 3.5/4.0 x 3mm |
| 00842092182307 - Equator | 2024-07-08 Equator Abutment for Astra TX 3.5/4.0 x 4mm |
Trademark Results [Straumann]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 STRAUMANN 78575002 3360454 Dead/Cancelled |
Straumann Holding AG 2005-02-25 |
 STRAUMANN 78455752 3708723 Live/Registered |
Straumann Holding AG 2004-07-23 |
 STRAUMANN 76533946 3043249 Live/Registered |
Straumann Holding AG 2003-07-31 |
 STRAUMANN 74505688 1998968 Live/Registered |
STRAUMANN HOLDING AG 1994-03-25 |
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