eudamed_udi
Primary ID: 04050598006201
MutaPLATE® Aldolase B™ (UDI 04050598006201)
Manufactured by Immundiagnostik AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MutaPLATE® Aldolase B™ - Primary ID 04050598006201
Device Regulatory Overview
The MutaPLATE® Aldolase B™ (Model/Catalog Number: KF190432) is a medical device manufactured by Immundiagnostik AG. This product is indexed under FDA Product Code / Category Classification W0106010499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KF190432
- Product Code / EMDN
- W0106010499
- Device Name
- MutaPLATE® Aldolase B™
- Database Sync Date
- 2026-08-09 16:46:20
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 MutaPLATE® Aldolase B™?
The registered manufacturer of record for MutaPLATE® Aldolase B™ is Immundiagnostik AG.
What is the Primary UDI-DI identifier for MutaPLATE® Aldolase B™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04050598006201.
What classification code is assigned to this device?
This device is registered under product classification code W0106010499.
Similar Classification Devices (W0106010499)
Other Devices by Immundiagnostik AG
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