Identity
- Trade Name
- Access Estradiol Calibrator S0 FDA UDI
- Generic Name
- Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- The Access Estradiol Calibrator S0 is intended for use with Access Estradiol assay to dilute patient samples containing analyte concentrations greater than the analyte specific S5 calibrator FDA UDI
- Model / Reference
- 33546 FDA UDI
- Description
- The Access Estradiol Calibrator S0 is intended for use with Access Estradiol assay to dilute patient samples containing analyte concentrations greater than the analyte specific S5 calibrator FDA UDI
Identifiers
- Catalog Number
- 33546 FDA UDI
- Primary DI / UDI-DI
- 15099590231385 FDA UDI
- FDA Product Code
- JIT FDA UDI
- GMDN Term
- Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA) 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
Yes
FDA UDI
Category: Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA)
Access Estradiol Calibrator S0 by Beckman Coulter, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Beckman Coulter, Inc.
Sources (1)
- FDA UDI 947032e1-812b-4a9a-9ebe-fad0c9d3d6b2 34 fields · synced Jun 8, 2026