A2-MACROGLOBULIN (UDI W0102019003)
Device Regulatory Overview
The A2-MACROGLOBULIN (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification W0102019003 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
- W0102019003
- Device Name
- A2-MACROGLOBULIN
- 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 A2-MACROGLOBULIN?
The registered manufacturer of record for A2-MACROGLOBULIN is .
What is the Primary UDI-DI identifier for A2-MACROGLOBULIN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W0102019003.
What classification code is assigned to this device?
This device is registered under product classification code W0102019003.
Similar Classification Devices (W0102019003)
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