Identity
- Trade Name
- ImmunoCAP Gliadin IgA Control High FDA UDI
- Generic Name
- Plasma protein IVD, control FDA UDI
- Device Name
- ImmunoCAP Gliadin IgA Control High FDA UDI
- Model / Reference
- 34-2332-51 FDA UDI
- Description
- ImmunoCAP Gliadin IgA Control High FDA UDI
Identifiers
- Catalog Number
- 34-2332-51 FDA UDI
- Primary DI / UDI-DI
- 07333066019918 FDA UDI
- 510(k) Number
- K052793 FDA UDI
- FDA Product Code
- MST FDA UDI
- GMDN Term
- Plasma protein IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5750 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
Category: Plasma protein IVD, control
ImmunoCAP Gliadin IgA Control High by Phadia GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K052793 also covers:
- ImmunoCAP Antigen AGf98, Gliadin — Phadia GmbH
- ImmunoCAP Gliadin IgA/IgG Control Low — Phadia GmbH
- ImmunoCAP Gliadin IgG Control High — Phadia GmbH
- ImmunoCAP Specific IgA Calibrators — Phadia GmbH
- ImmunoCAP Specific IgA Conjugate — Phadia GmbH
- ImmunoCAP Specific IgA Curve Controls — Phadia GmbH
- ImmunoCAP Specific IgA/IgG Sample Diluent — Phadia GmbH
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Phadia GmbH
Sources (1)
- FDA UDI 5e7dc6ec-0520-4b72-a250-f416898c531f 37 fields · synced Jun 8, 2026