| Primary Device ID | 07640159550082 |
| NIH Device Record Key | 8b5adc32-d748-4332-ab64-87a9a8019e1d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5m |
| Version Model Number | 501-6535 |
| Company DUNS | 486405637 |
| Company Name | Lanterna Medical Technologies GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 |
| Phone | +41712800930 |
| info@lanternamedtech.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07640159550082 [Primary] |
| NKB | Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07640159550082]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2014-09-03 |
| 07640159550129 | Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.55mm |
| 07640159550112 | Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.50mm |
| 07640159550105 | Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.45mm |
| 07640159550099 | Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.40mm |
| 07640159550082 | Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.35mm |