| Primary Device ID | 06430035872978 |
| NIH Device Record Key | 446edf8d-db0a-4a92-a159-d69d3895e7ec |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KAVO X PRO REUSABLE TIP SUPPORT |
| Version Model Number | 901129 |
| Company DUNS | 459955188 |
| Company Name | PaloDEx Group Oy |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06430035872978 [Primary] |
| NOF | System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-11-07 |
| Device Publish Date | 2019-10-30 |
| 06430035875191 - ORTHOPANTOMOGRAPH™ OP 3D | 2025-07-23 OP 3D EX CEPH UPGRADE KIT |
| 06430035875184 - ORTHOPANTOMOGRAPH™ OP 3D | 2025-03-19 ORTHOPANTOMOGRAPH™ OP 3D EX (PAN CEPH 3D) |
| 06430035872947 - OCCLUSAL 4C START-UP KIT | 2024-07-25 OCCLUSAL 4C START-UP KIT |
| 06430035875177 - ORTHOPANTOMOGRAPH™ OP 3D | 2024-05-14 ORTHOPANTOMOGRAPH™ OP 3D EX (PAN 3D) |
| 06430035875139 - ORTHOPANTOMOGRAPH™ OP 3D | 2024-03-22 OP 3D LX CEPH UPGRADE KIT |
| 06430035875092 - ORTHOPANTOMOGRAPH™ OP 3D | 2023-10-10 ORTHOPANTOMOGRAPH™ OP 3D LX (PAN 3D) |
| 06430035875108 - ORTHOPANTOMOGRAPH™ OP 3D | 2023-10-10 ORTHOPANTOMOGRAPH™ OP 3D LX (PAN, CEPH 3D) |
| 06430035873630 - Orthopantomograph OP 3D | 2021-06-08 |