Identity
- Trade Name
- Alinity FDA UDI
- Generic Name
- Progesterone IVD, calibrator FDA UDI
- Device Name
- Alinity i Progesterone Calibrators FDA UDI
- Model / Reference
- 08P3601 FDA UDI
- Description
- Alinity i Progesterone Calibrators FDA UDI
Identifiers
- Catalog Number
- 08P3601 FDA UDI
- Primary DI / UDI-DI
- 00380740121853 FDA UDI
- FDA Product Code
- JIT FDA UDI
- GMDN Term
- Progesterone IVD, calibrator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1150 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
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, calibrator
Alinity by Abbott Ireland — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Progesterone IVD, calibrator.
- Elecsys Progesterone III CalSet — Roche Diagnostics Corp. · Class II
- ST AIA-PACK PROG II CALIBRATOR SET — Tosoh Corp. · Class II
- IDS-iSYS 17-OH Progesterone Calibration Verifiers — Immunodiagnostic Systems , Ltd. · Class I
- Dimension Vista® PROG Calibrator — Siemens Healthcare Diagnostics · Class II
- ARCHITECT — ABBOTT IRELAND · Class II
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
- Abbott Ireland
Sources (1)
- FDA UDI ee0572f5-dd65-4aa9-96e9-c794767ced88 36 fields · synced May 31, 2026