MutaPLATE® VDR BsmI Real-Time-PCR-Kit (UDI 04050598002241)
Manufactured by Immundiagnostik AG
Device Regulatory Overview
The MutaPLATE® VDR BsmI Real-Time-PCR-Kit (Model/Catalog Number: KF1900432) 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
- KF1900432
- Product Code / EMDN
- W0106010499
- Device Name
- MutaPLATE® VDR3/Bsm1 ™, PCR
- Database Sync Date
- 2026-08-09 16:49:10
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® VDR BsmI Real-Time-PCR-Kit?
The registered manufacturer of record for MutaPLATE® VDR BsmI Real-Time-PCR-Kit is Immundiagnostik AG.
What is the Primary UDI-DI identifier for MutaPLATE® VDR BsmI Real-Time-PCR-Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04050598002241.
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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