| Primary Device ID | 07640161396500 |
| NIH Device Record Key | df7511be-87a9-4dcd-9991-52abf96b9d52 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CERALOG PL Implant, Ø 5.0 L 13 |
| Version Model Number | HP1040.5013 |
| Catalog Number | HP1040.5013 |
| Company DUNS | 483229493 |
| Company Name | Dentalpoint AG |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07640161396500 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-07 |
| Device Publish Date | 2024-04-29 |
| 07640161393769 - ZERAMEX®XT Rescue-Shell XT REGULAR | 2024-05-15 ZERAMEX®XT Rescue-Shell XT REGULAR |
| 07640161393776 - ZERAMEX®XT Rescue-Shell XT WIDE | 2024-05-15 ZERAMEX®XT Rescue-Shell XT WIDE |
| 07640161395077 - ZERAMEX®XT Rescue-Shell XT SMALL | 2024-05-15 ZERAMEX®XT Rescue-Shell XT SMALL |
| 07640161396401 - CERALOG PL Implant, Ø 3.8 L 9 | 2024-05-07 Dental Implant |
| 07640161396432 - CERALOG PL Implant, Ø 3.8 L 11 | 2024-05-07 Dental Implant |
| 07640161396449 - CERALOG PL Implant, Ø 3.8 L 13 | 2024-05-07 Dental Implant |
| 07640161396456 - CERALOG PL Implant, Ø 4.3 L 9 | 2024-05-07 Dental Implant |
| 07640161396463 - CERALOG PL Implant,Ø 4.3 L 11 | 2024-05-07 Dental Implant |