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DIO Multi Unit Abutment Holder
EUDAMEDFDA UDIClass I (EU MDR)
Ref MAH 1425Model ASC 1511
Identity
- Trade Name
- DIO Multi Unit Abutment Holder EUDAMEDFDA UDI
- Generic Name
- Dental implant/prosthesis handling forceps FDA UDI
- Device Name
- DIOnavi. Anchor Screw EUDAMED
- Model / Reference
- ASC 1511 EUDAMEDMAH 1425 EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800049286470 EUDAMEDFDA UDI
- Basic UDI-DI
- 880004921004AA EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- Q010399 SURGICAL DENTAL DEVICES - OTHER EUDAMED
- GMDN Term
- Dental implant/prosthesis handling forceps FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Market of Registration
- Portugal EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
DIO Multi Unit Abutment Holder by DIO Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 880004921004AA | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- DIO Corporation
- EUDAMED SRN
- KR-MF-000008515
- Authorised Representative
- AR Experts B.V. NL-AR-000023989
Sources (2)
- EUDAMED 25eb8d07-d056-42dc-9527-0c22e6a59b94 61 fields · synced Jul 9, 2026
- FDA UDI b6b721ac-365c-42e7-beb1-a1a5908be254 32 fields · synced May 30, 2026