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Modified Gliadin Peptide IgG ELISA
EUDAMEDClass IVD General (EU MDR)
Ref RE75751
Identity
- Trade Name
- Modified Gliadin Peptide IgG ELISA EUDAMED
- Device Name
- Modified Gliadin Peptide IgG ELISA EUDAMED
- Model / Reference
- RE75751 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04049325005860 EUDAMED
- Basic UDI-DI
- B-04049325005860 EUDAMED
- EMDN Code
- W0102100604 GLIADIN ANTIBODIES EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
Yes
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Modified Gliadin Peptide IgG ELISA by Ibl International Gmbh — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-04049325005860 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- IBL International GmbH
- EUDAMED SRN
- DE-MF-000015709
Sources (1)
- EUDAMED 5273b1d2-d3cf-420f-ad48-229ea78eb21d 61 fields · synced Sep 17, 2026