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ACCURUN 135 Toxoplasma IgG Positive Control
EUDAMEDFDA UDIClass IVD Annex II List B (EU MDR)
Ref 2015-0082
Identity
- Trade Name
- ACCURUN 135 Toxoplasma IgG Positive Control EUDAMEDACCURUN® FDA UDI
- Generic Name
- Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control FDA UDI
- Device Name
- ACCURUN 135 Toxoplasma IgG Positive Control EUDAMEDACCURUN 135 Toxoplasma IgG 1 x 1.0 mL FDA UDI
- Model / Reference
- 2015-0082 EUDAMEDFDA UDI
- Description
- ACCURUN 135 Toxoplasma IgG 1 x 1.0 mL FDA UDI
Identifiers
- Catalog Number
- 2015-0082 FDA UDI
- Primary DI / UDI-DI
- 00816784020390 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00816784020390 EUDAMED
- 510(k) Number
- K974261 FDA UDI
- FDA Product Code
- LJK FDA UDI
- EMDN Code
- W0105080805 PARASITOLOGY CONTROLS - INF.IMM. EUDAMED
- GMDN Term
- Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control FDA UDI
Classification
- Device Class
- Class IVD Annex II List B EUDAMEDClass II FDA UDI
- Regulation Number
- 866.3780 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
ACCURUN 135 Toxoplasma IgG Positive 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-00816784020390 | Class IVD Annex II List B | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD Annex II List B | Pending data |
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Manufacturer
- Manufacturer
- LGC Clinical Diagnostics, Inc.
- EUDAMED SRN
- US-MF-000016356
- Authorised Representative
- MediMark Europe Sarl. FR-AR-000000182
Sources (2)
- EUDAMED 735ee4bf-0aa6-4209-9f25-b37ac3949cb4 61 fields · synced Jun 19, 2026
- FDA UDI 87a13d31-e69a-40c3-9859-be934046ac3d 36 fields · synced May 30, 2026