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Roll Wave
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref D-P.01.10-025-06-035-GD-000-00-00Model Roll Wave Gold 25mm Medium#035/06 4pcs/packRef D-P.01.10-025-05-045-GD-000-00-00Model Roll Wave Gold 25mm Large#045/05 4pcs/packRef D-P.01.10-021-06-035-GD-000-00-00Model Roll Wave Gold 21mm Medium#035/06 4pcs/pack
Identity
- Trade Name
- Roll Wave EUDAMEDDenco FDA UDI
- Generic Name
- Rotary/reciprocating endodontic file/rasp, single-use FDA UDI
- Device Name
- Roll Wave EUDAMED
- Model / Reference
- Roll Wave Gold 25mm Medium#035/06 4pcs/pack EUDAMEDD-P.01.10-025-06-035-GD-000-00-00 EUDAMEDRoll Wave Gold 25mm Large#045/05 4pcs/pack EUDAMEDD-P.01.10-025-05-045-GD-000-00-00 EUDAMEDRoll Wave Gold 21mm Medium#035/06 4pcs/pack EUDAMEDD-P.01.10-021-06-035-GD-000-00-00 EUDAMED25mm Roll Wave 35/6% Medium 4pcs/pack FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06970514918846 EUDAMEDFDA UDI06970514918853 EUDAMED06975718056387 EUDAMED
- Basic UDI-DI
- B-06970514918846 EUDAMEDB-06970514918853 EUDAMEDB-06975718056387 EUDAMED
- FDA Product Code
- EKS FDA UDI
- EMDN Code
- Q010507 ENDODONTIC INSTRUMENTS (CANAL ENLARGERS, FILES, RASPS, ETC.), SINGLE-USE EUDAMED
- GMDN Term
- Rotary/reciprocating endodontic file/rasp, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Market of Registration
- Türkiye EUDAMED
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Roll Wave by Shenzhen Denco Medical Co., Ltd. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06970514918846 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Shenzhen Denco Medical Co., Ltd.
- EUDAMED SRN
- CN-MF-000014271
- Authorised Representative
- Share info GmbH DE-AR-000005132
Sources (4)
- EUDAMED b6230ff8-2794-4b8b-a395-6cdc3dd9a2f8 61 fields · synced Aug 1, 2026
- EUDAMED ad0b4577-848e-426e-a8c2-e858fbbc4bee 61 fields · synced May 17, 2026
- EUDAMED 828b885d-5f9c-45b9-80cd-bc0edfddf4df 61 fields · synced May 18, 2026
- FDA UDI ec065383-aaac-4895-afe5-215968900160 33 fields · synced May 30, 2026