← Back to catalogue
ACCURUN 800 ToRCH Negative Control
EUDAMEDFDA UDIClass IVD Annex II List B (EU MDR)
Ref 2010-0018
Identity
- Trade Name
- ACCURUN 800 ToRCH Negative Control EUDAMEDACCURUN® FDA UDI
- Generic Name
- Negative control immunoglobulin IVD FDA UDI
- Device Name
- ACCURUN 800 ToRCH Negative Control EUDAMEDACCURUN 800 ToRCH 1 x 1.0 mL FDA UDI
- Model / Reference
- 2010-0018 EUDAMEDFDA UDI
- Description
- ACCURUN 800 ToRCH 1 x 1.0 mL FDA UDI
Identifiers
- Catalog Number
- 2010-0018 FDA UDI
- Primary DI / UDI-DI
- 00816784020239 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00816784020239 EUDAMED
- FDA Product Code
- DGQ FDA UDI
- EMDN Code
- W0105080899 CONTROLS - INF. IMMUNOLOGY - OTHER EUDAMED
- GMDN Term
- Negative control immunoglobulin IVD FDA UDI
Classification
- Device Class
- Class IVD Annex II List B EUDAMEDClass I FDA UDI
- Regulation Number
- 866.5700 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
Yes
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
Yes
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
ACCURUN 800 ToRCH Negative Control by LGC Clinical Diagnostics, Inc. — Class IVD Annex II List B — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-00816784020239 | Class IVD Annex II List B | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD Annex II List B | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- LGC Clinical Diagnostics, Inc.
- EUDAMED SRN
- US-MF-000016356
- Authorised Representative
- MediMark Europe Sarl. FR-AR-000000182
Sources (2)
- EUDAMED 99641218-8a6e-48d6-9b1c-6e85503019c7 61 fields · synced Jun 19, 2026
- FDA UDI e9760ceb-93d5-4d4a-9782-8a67980ed88e 35 fields · synced May 29, 2026