Primary Device ID | E219J302648001 |
NIH Device Record Key | 9d4c1aa5-fd1a-430a-9a39-9a6cfd39f92e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multi-unit Implant analog |
Version Model Number | J3026.4800 |
Catalog Number | J3026.4800 |
Company DUNS | 322018193 |
Company Name | ALTATEC GmbH |
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 | 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 |
E219J302648001 - Multi-unit Implant analog | 2024-12-25Multi-unit Implant analog |
E219J302648001 - Multi-unit Implant analog | 2024-12-25 Multi-unit Implant analog |
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E219C244133201 - CONELOG® CAM Titan. Blank, type ME | 2024-06-06 CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 3.3 mm, L 20.0 mm, 2 units |
E219C244138201 - CONELOG® CAM Titan. Blank, type ME | 2024-06-06 CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 3.8 mm, L 20.0 mm, 2 units |