eudamed_udi
Primary ID: 06438147331000
DELFIA/AutoDELFIA PlGF kit (UDI 06438147331000)
Manufactured by Wallac Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DELFIA/AutoDELFIA PlGF kit - Primary ID 06438147331000
Device Regulatory Overview
The DELFIA/AutoDELFIA PlGF kit (Model/Catalog Number: B055-201) is a medical device manufactured by Wallac Oy. This product is indexed under FDA Product Code / Category Classification W0102050299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B055-201
- Product Code / EMDN
- W0102050299
- Device Name
- DELFIA/AutoDELFIA PlGF kit
- Database Sync Date
- 2026-08-09 16:29:15
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 DELFIA/AutoDELFIA PlGF kit ?
The registered manufacturer of record for DELFIA/AutoDELFIA PlGF kit is Wallac Oy.
What is the Primary UDI-DI identifier for DELFIA/AutoDELFIA PlGF kit ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438147331000.
What classification code is assigned to this device?
This device is registered under product classification code W0102050299.
Similar Classification Devices (W0102050299)
Other Devices by Wallac Oy
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