| Primary Device ID | 06009544004820 |
| NIH Device Record Key | c2bfe880-d38e-487e-9ab6-c384dc19f31d |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | DCT3009 |
| Company DUNS | 636239584 |
| Company Name | SOUTHERN IMPLANTS (PTY) 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 | 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 | 06009544004820 [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 | 2019-01-07 |
| Device Publish Date | 2018-12-05 |
| 06009544027638 - N/A | 2025-04-10 Resorbable collagen membrane 15x20mm |
| 06009544027645 - N/A | 2025-04-10 Resorbable collagen membrane 20x30mm |
| 06009544027652 - N/A | 2025-04-10 Resorbable collagen membrane 30x40mm |
| 06009544027669 - N/A | 2025-04-10 Bone matrix, porcine cancellous fine 0.5cc |
| 06009544027676 - N/A | 2025-04-10 Bone matrix, porcine cancellous fine 1.0cc |
| 06009544027683 - N/A | 2025-04-10 Bone matrix, porcine cancellous fine 2.0cc |
| 06009544027690 - N/A | 2025-04-10 Bone matrix, porcine cancellous std 2.0cc |
| 06009544027706 - N/A | 2025-04-10 Bone matrix, porcine cancellous std 1.0cc |