Articulating Film Blue
by Rayson Healthcare, Inc DBA Raydenco, Inc.
Ref 20 55 7501Model 20 55 7509
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 | Number0817807filmblue126D 00817807000429 | 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- Withdrawn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
- Blue Articulating Film
- Model / Reference
- 20 55 7509, 20 55 7501
- Primary DI / UDI-DI
- 00817807000429
- Basic UDI-DI
- 0817807filmblue126D
- Direct Marketing DI
- 00817807000429
- 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