K3Pro Standard Aufbau
by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG 22 variants
Ref EAK 401015.VH/2ProModel 4.0 x 1.5mm 10° Preform Abutment with 2mm Post - solid
Active
CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-EAGNEAK401015VH2ORO0 EAGNEAK401015VH2ORO0 | Date24 Apr 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Model / Reference
- 4.0 x 1.5mm 10° Preform Abutment with 2mm Post - solid, EAK 401015.VH/2Pro
- Primary DI / UDI-DI
- EAGNEAK401015VH2ORO0
- Basic UDI-DI
- B-EAGNEAK401015VH2ORO0
- EMDN Code
- P01020101 Dental implants
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000012472
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Properties
Other properties (12)
- Sterile: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No