| Primary Device ID | 07290109742410 |
| NIH Device Record Key | 627b61d2-50d5-4a63-88a6-a55641f085ea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IN Abutment 4.5 X 9 |
| Version Model Number | 1 |
| Catalog Number | BH-IB39 |
| Company DUNS | 600330916 |
| Company Name | BHI IMPLANTS LTD |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +972046094458 |
| info@bh-implants.com |
| Length | 9 Millimeter |
| Handling Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290109742410 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07290109742410]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-04-01 |
| Device Publish Date | 2020-03-24 |
| 07290109747699 - Bhi Implants | 2025-12-18 QT EQUATOR SCREW VENT h1 |
| 07290109747705 - Bhi Implants | 2025-12-18 QT EQUATOR SCREW VENT h2 |
| 07290109747712 - Bhi Implants | 2025-12-18 QT EQUATOR SCREW VENT h3 |
| 07290109747729 - Bhi Implants | 2025-12-18 QT EQUATOR SCREW VENT h4 |
| 07290109747736 - Bhi Implants | 2025-12-18 QT EQUATOR SCREW VENT h0.5 |
| 07290109747743 - Bhi Implants | 2025-12-18 Twist Drill 3.0 L 16 |
| 07290109747750 - Bhi Implants | 2025-12-18 Special tools and accessories collection |
| 07290109747767 - Bhi Implants | 2025-12-18 Marking Drill |