Optilite® C4 Control Pack
by The Binding Site Group Ltd EUDAMEDGUDID
Active
Ref NQ025.OPTModel NK025.OPT
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDR EUDAMED | Number5051700NK025.OPT5Z | Date18 Nov 2025 | StatusActive |
| United States | GUDID listing GUDID | Number05051700019088 | Date2 Aug 2017 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Generic Name
- Complement components C4/C4c IVD, control
- Device Name
- Optilite® C4 Kit
- Model / Reference
- NK025.OPT, NQ025.OPT
- Primary DI / UDI-DI
- 05051700019088
- Basic UDI-DI
- 5051700NK025.OPT5Z
- FDA Product Code
- JJX
- EMDN Code
- W0102010205 Complement component c4
- GMDN Term
- Complement components C4/C4c IVD, control
- Device Class
- Class B EUDAMEDClass I GUDID
- Regulation Number
- 862.1660
- Market of Registration
- Germany
- Commercial Distribution
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class B | Class I |
Manufacturer details
- EUDAMED SRN
- UK-MF-000036707
- Authorised representative
- The Binding Site Ireland Limited IE-AR-000034426
Other devices from The Binding Site Group Ltd.
Properties
Other properties (16)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Microbial Substances: No
- Self Testing: No
- Near-Patient Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No
- New Device: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No