Identity
- Trade Name
- DuraCetal EUDAMEDFDA UDI
- Generic Name
- Dental appliance fabrication material, thermoplastic FDA UDI
- Device Name
- Thermoplastic denture base resin EUDAMEDShade A2 225g Bottle Thermoplastic Dental Resin FDA UDI
- Model / Reference
- ACE-A20-270-B08 EUDAMEDFDA UDI
- Description
- Shade A2 225g Bottle Thermoplastic Dental Resin FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00842326102804 EUDAMEDFDA UDI
- Basic UDI-DI
- 08423261ThermoplasticDR5S EUDAMED
- FDA Product Code
- EBI FDA UDIEHP FDA UDI
- EMDN Code
- Q0102050102 DENTAL REBASING RESINS EUDAMED
- GMDN Term
- Dental appliance fabrication material, thermoplastic FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 872.3760 FDA UDI872.3285 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
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
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
Dimensions & Sizes
- Size
- Weight — 225 Gram FDA UDI
DuraCetal by The Myerson Company Limited — Class I — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K172407 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 08423261ThermoplasticDR5S | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- The Myerson Company Limited
- EUDAMED SRN
- TT-MF-000045141
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (3)
- EUDAMED 38b49c5d-f0e8-413c-b197-d6297a69d313 61 fields · synced Jul 13, 2026
- FDA UDI ae0e0fd7-7fb7-4746-b811-98dcec6ff406 35 fields · synced May 30, 2026
- FDA 510(k) K172407 1 fields · synced May 18, 2026