| Primary Device ID | 07290109742359 |
| NIH Device Record Key | a12f9636-c938-4576-92f2-1637d58861a9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IN Abutment 3.5 X 7 |
| Version Model Number | 1 |
| Catalog Number | BH-IB27 |
| 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 | 7 Millimeter |
| Handling Environment Temperature | Between 5 Degrees Celsius and 40 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290109742359 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07290109742359]
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 |
| 07290109747781 - OsseoPress® | 2026-01-16 OsseoPress Drill Dia 2.25 |
| 07290109747798 - OsseoPress® | 2026-01-16 OsseoPress Drill Dia 2.50 |
| 07290109747804 - OsseoPress® | 2026-01-16 OsseoPress Drill Dia 2.75 |
| 07290109747811 - OsseoPress® | 2026-01-16 OsseoPress Drill Dia 3.00 |
| 07290109747828 - OsseoPress® | 2026-01-16 OsseoPress Drill Dia 3.25 |
| 07290109747835 - OsseoPress® | 2026-01-16 OsseoPress Drill Dia 3.50 |
| 07290109747842 - OsseoPress® | 2026-01-16 OsseoPress Drill Dia 3.75 |
| 07290109747859 - OsseoPress® | 2026-01-16 OsseoPress Drill Dia 4.00 |