Nitrocare Pedi̇atri̇k Hasta Karyolasi
by Nitrocare Medi̇kal Mobi̇lya Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ 10 variants
Ref NHB 2130PModel NITRO HB 6440
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 | Number869925869NTRCBEDMX 08699258691904 | Date3 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- Withdrawn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
- Motorized Patient Bed
- Model / Reference
- NITRO HB 6440, NHB 2130P
- Primary DI / UDI-DI
- 08699258691904
- Basic UDI-DI
- 869925869NTRCBEDMX
- Direct Marketing DI
- 08699258691904
- EMDN Code
- V0806010701 Hospital/home care pediatric electric medical beds
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000044596
Other devices from Nitrocare Medi̇kal Mobi̇lya Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇
See all devices from Nitrocare Medi̇kal Mobi̇lya Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ →
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