Hiossen® HG-compatible 8005151
GUDID 00842092115374
Hiossen® HG-compatible Regular Guide Pin
Preat Corporation
Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use Dental prosthesis/implant abutment screw analog, single-use| Primary Device ID | 00842092115374 |
| NIH Device Record Key | 4467c406-5344-45bb-96d9-3162d84dd869 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hiossen® HG-compatible |
| Version Model Number | 8005151 |
| Catalog Number | 8005151 |
| 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 | false |
| 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 | |
| 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 | 00842092115374 [Primary] |
FDA Product Code
| NDP | Accessories, Implant, Dental, Endosseous |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
[00842092115374]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-18 |
| Device Publish Date | 2023-08-10 |
On-Brand Devices [Hiossen® HG-compatible]
| 00842092115374 | Hiossen® HG-compatible Regular Guide Pin |
| 00842092125243 | Hiossen® HG-compatible Standard Blue Light Scan Body |
Trademark Results [Hiossen]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HIOSSEN 77264620 3547792 Live/Registered |
OSSTEM IMPLANT, CO., LTD. 2007-08-27 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.