ALPHAFETOPROTEIN (UDI W0102039001)
Device Regulatory Overview
The ALPHAFETOPROTEIN (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification W0102039001 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- W0102039001
- Device Name
- ALPHAFETOPROTEIN
- Database Sync Date
- 2026-08-09 16:18:37
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ALPHAFETOPROTEIN?
The registered manufacturer of record for ALPHAFETOPROTEIN is .
What is the Primary UDI-DI identifier for ALPHAFETOPROTEIN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W0102039001.
What classification code is assigned to this device?
This device is registered under product classification code W0102039001.
Similar Classification Devices (W0102039001)
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