Raycome
by Shenzhen Raycome Health Technology Co., Ltd 9 variants
Ref RBP-7000Model RBP-7000,RBP-7000B,RBP-7000W,RBP-9000,RBP-9000c
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number69541601AUTO01NX 06954160100572 | Date8 Sep 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Automatic PulseWave Blood Pressure Monitor
- Model / Reference
- RBP-7000, RBP-7000B, RBP-7000W, RBP-9000, RBP-9000c
- Primary DI / UDI-DI
- 06954160100572
- Basic UDI-DI
- 69541601AUTO01NX
- Direct Marketing DI
- 06954160100572
- EMDN Code
- Z1203020302 Non–invasive blood pressure monitoring instruments
- Device Class
- Class IIa
- EU market of registration
- Poland
Manufacturer details
- EUDAMED SRN
- CN-MF-000033181
- Authorised representative
- Lotus NL B.V. NL-AR-000000121
Other devices from Shenzhen Raycome Health Technology Co., Ltd
See all devices from Shenzhen Raycome Health Technology Co., Ltd →
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Incorporates Medicinal Product: No