Identity
- Trade Name
- Pantex P674SE FDA UDI
- Generic Name
- Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- Salivary 17ß-Estradiol EIA Antibody FDA UDI
- Model / Reference
- P674SE FDA UDI
- Description
- Salivary 17ß-Estradiol EIA Antibody FDA UDI
Identifiers
- Catalog Number
- 674 FDA UDI
- Primary DI / UDI-DI
- 00850039602429 FDA UDI
- GMDN Term
- Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- 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: Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA)
Pantex P674SE by Pantex — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Pantex
Sources (1)
- FDA UDI 85d984c1-ffa0-444b-8a0b-7827ed55a702 36 fields · synced May 31, 2026