Identity
- Trade Name
- Progesterone ELISA FDA UDI
- Generic Name
- Progesterone IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- Intended for the direct quantitative determination of Progesterone by enzyme immunoassay using human serum. For in vitro diagnostic use. FDA UDI
- Model / Reference
- 11-PROHU-E01 FDA UDI
- Description
- Intended for the direct quantitative determination of Progesterone by enzyme immunoassay using human serum. For in vitro diagnostic use. FDA UDI
Identifiers
- Catalog Number
- 11-PROHU-E01 FDA UDI
- Primary DI / UDI-DI
- B24211PROHUE010 FDA UDI
- FDA Product Code
- JLS FDA UDI
- GMDN Term
- Progesterone IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1620 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Progesterone IVD, kit, enzyme immunoassay (EIA)
Progesterone ELISA by American Laboratory Products Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Progesterone IVD, kit, enzyme immunoassay (EIA).
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- Pantex P637SP — Pantex
- Progesterone AccuBind ELISA Test System - 96 Wells — MONOBIND, INC. · Class I
- Salivary Progesterone ELISA — DRG International, Inc. · Class I
- Pantex — Pantex · Class I
- Pantex P637SP — Pantex
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
- American Laboratory Products Company
Sources (1)
- FDA UDI a0ee0259-b762-482c-b2bd-15fddcc5915e 36 fields · synced May 31, 2026