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Diaplus
EUDAMEDFDA UDIFDA 510(k)Class IIa (EU MDR)
Ref A2001-2101Model DIAPLUS 5ml
Identity
- Trade Name
- DIAPLUS EUDAMEDFDA UDI
- Generic Name
- Dentine bonding agent/set FDA UDI
- Device Name
- DIAPLUS EUDAMEDDiaPlus is a photopolymerization type dentine and enamel adhesive as a 5th generation dentine adhesion system that can be applied to all types of composite resin restorations. FDA UDI
- Model / Reference
- DIAPLUS 5ml EUDAMEDFDA UDIA2001-2101 EUDAMED
- Description
- DiaPlus is a photopolymerization type dentine and enamel adhesive as a 5th generation dentine adhesion system that can be applied to all types of composite resin restorations. FDA UDI
Identifiers
- Catalog Number
- A2001-2101 FDA UDI
- Primary DI / UDI-DI
- 08806383565141 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08806383565141 EUDAMED
- FDA Product Code
- KLE FDA UDI
- EMDN Code
- Q01010104 DENTAL BONDING AGENTS EUDAMED
- GMDN Term
- Dentine bonding agent/set FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 872.3200 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dentine bonding agent/set
Diaplus by Diadent Group International — Class IIa — FDA_510K, MDD — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
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Also classified as Dentine bonding agent/set.
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Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K192392 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-08806383565141 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Diadent Group International
- EUDAMED SRN
- KR-MF-000023806
- Authorised Representative
- Diadent Europe B.V. NL-AR-000012597
Sources (3)
- EUDAMED 97928488-4d0d-4efb-8205-e6f5c21fce11 61 fields · synced Jul 28, 2026
- FDA UDI cf8560f9-6442-4f85-9892-37541a866f71 35 fields · synced May 30, 2026
- FDA 510(k) K192392 1 fields · synced May 18, 2026