Articulating Film Red/Blue Combo
by Rayson Healthcare, Inc DBA Raydenco, Inc.
Ref 20 55 7507
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 | Number0817807filmcombo3J 00817807000436 | Date23 Jul 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- Withdrawn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
- Red/Blue Articulating Film
- Model / Reference
- 20 55 7507
- Primary DI / UDI-DI
- 00817807000436
- Basic UDI-DI
- 0817807filmcombo3J
- Direct Marketing DI
- 00817807000436
- EMDN Code
- Q01020201 Articulation papers
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- US-MF-000052071
- Authorised representative
- Obelis s.a. BE-AR-000000106
From the manufacturer
Manufacturer's product page: Articulating Film
Other devices from Rayson Healthcare, Inc DBA Raydenco, Inc.
See all devices from Rayson Healthcare, Inc DBA Raydenco, Inc. →
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