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Hollowware
EUDAMEDClass I (EU MDR)
Ref DDP-D8-282Ref DDP-D8-182ARef DDP-D8-159Ref DDP-D8-49
by Daddy D Pro
Identity
- Device Name
- HOLLOWWARE EUDAMED
- Model / Reference
- DDP-D8-282 EUDAMEDDDP-D8-182A EUDAMEDDDP-D8-159 EUDAMEDDDP-D8-49 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +B961DDPD82820 EUDAMED+B961DDPD8182A0/$26678/16D202508035 EUDAMED+B961DDPD81590/$26783/16D202509071 EUDAMED+B961DDPD8490 EUDAMED
- Basic UDI-DI
- ++B961HOLLOWWARE9H EUDAMED
- EMDN Code
- Q010399 SURGICAL DENTAL DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
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
Yes
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Hollowware by Daddy D Pro — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++B961HOLLOWWARE9H | Class I | Active |
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Manufacturer
- Manufacturer
- Daddy D Pro
- EUDAMED SRN
- PK-MF-000035172
- Authorised Representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Sources (4)
- EUDAMED 6f9f53ee-a3d1-4c14-87ec-5de4e7bfc2e5 61 fields · synced Sep 18, 2026
- EUDAMED 50d5c67f-4524-49a9-82fe-168881b605f6 61 fields · synced May 17, 2026
- EUDAMED 920b12b2-f869-4ada-bfae-4d7148e6f1fc 61 fields · synced May 18, 2026
- EUDAMED b0aca8f5-9b61-451a-8f13-0758fab07ce8 61 fields · synced May 18, 2026