Identity
- Trade Name
- Pregnenolone ELISA FDA UDI
- Generic Name
- Pregnenolone IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- For the quantitative measurement of Pregnenolone in human serum by an ELISA (Enzyme-Linked Immunosorbent Assay). FDA UDI
- Model / Reference
- IB59107 FDA UDI
- Description
- For the quantitative measurement of Pregnenolone in human serum by an ELISA (Enzyme-Linked Immunosorbent Assay). FDA UDI
Identifiers
- Catalog Number
- IB59107 FDA UDI
- Primary DI / UDI-DI
- B652IB59107 FDA UDI
- FDA Product Code
- JNG FDA UDI
- GMDN Term
- Pregnenolone IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1615 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Pregnenolone IVD, kit, enzyme immunoassay (EIA)
Pregnenolone ELISA by IBL America — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pregnenolone IVD, kit, enzyme immunoassay (EIA).
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 I | Pending data |
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Manufacturer
- Manufacturer
- IBL America
Sources (1)
- FDA UDI 18554e3a-9c9d-4598-b3ed-dba6e1defeb8 36 fields · synced May 30, 2026