STANDALONE ANTI-DECUBITUS MATTRESS RehaComfort
by REHA FUND Sp. z o.o. 6 variants
Ref RF-C1/12/EN, RF-C1/15/N, RF-C1/12/N, RF-C1/10/EN, RF-C1/12/BEN, RF-C1/15/BEN, RF-C1/10/NModel RF-C1
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number59039407RFC1R5 | Date20 Apr 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- MATERAC PRZECIWODLEŻYNOWY SAMODZIELNY RehaComfort
- Model / Reference
- RF-C1, RF-C1/12/EN, RF-C1/15/N, RF-C1/12/N, RF-C1/10/EN, RF-C1/12/BEN, RF-C1/15/BEN, RF-C1/10/N
- Primary DI / UDI-DI
- 05903940713298, 05903940713366, 05903940713359, 05903940713281, 05903940713328, 05903940713335, 05903940713342
- Basic UDI-DI
- 59039407RFC1R5
- Direct Marketing DI
- 05903940713298059039407133660590394071335905903940713281059039407133280590394071333505903940713342
- EMDN Code
- V080702 Non active anti-decubitus medical mattresses
- Device Class
- Class I
- EU market of registration
- Poland
Manufacturer details
- EUDAMED SRN
- PL-MF-000047481
Other devices from REHA FUND Sp. z o.o.
Properties
Other properties (13)
- 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
- Measuring Function: No
- Incorporates Medicinal Product: No