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Rollator
EUDAMEDClass I (EU MDR)
Ref ZBR018Model ZBR001, ZBR002, ZBR003, ZBR004, ZBR005, ZBR006, ZBR007, ZBR008, ZBR009, ZBR010, ZBR011, ZBR012, ZBR013, ZBR014, ZBR015, ZBR016, ZBR017, ZBR018, ZBR019, ZBR020, ZBR021, ZBR022, ZBR023, ZBR024, ZBR025, ZBR026, ZBR027, etc
Identity
- Device Name
- Rollator EUDAMED
- Model / Reference
- ZBR001, ZBR002, ZBR003, ZBR004, ZBR005, ZBR006, ZBR007, ZBR008, ZBR009, ZBR010, ZBR011, ZBR012, ZBR013, ZBR014, ZBR015, ZBR016, ZBR017, ZBR018, ZBR019, ZBR020, ZBR021, ZBR022, ZBR023, ZBR024, ZBR025, ZBR026, ZBR027, etc EUDAMEDZBR018 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06973608040188 EUDAMED
- Basic UDI-DI
- 697360804ZBROR8 EUDAMED
- EMDN Code
- Y120606 WHEELED WALKER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Rollator by Foshan Zubon Technology Co., Ltd — 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 | 697360804ZBROR8 | Class I | Active |
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Manufacturer
- Manufacturer
- Foshan Zubon Technology Co., Ltd
- EUDAMED SRN
- CN-MF-000045637
- Authorised Representative
- SUNGO Europe B.V. NL-AR-000000247
Sources (1)
- EUDAMED 44947a1d-b539-48df-9af7-a4b572a98414 61 fields · synced Jun 18, 2026