nal von minden Drug-Screen® FYL 10 Test (UDI D-nvm-101029Q4)
Manufactured by nal von minden GmbH
Device Regulatory Overview
The nal von minden Drug-Screen® FYL 10 Test (Model/Catalog Number: 101029) is a medical device manufactured by nal von minden GmbH. This product is indexed under FDA Product Code / Category Classification W0102160508 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 101029
- Product Code / EMDN
- W0102160508
- Device Name
- FYL 10 Test
- Database Sync Date
- 2026-08-09 16:48:49
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 nal von minden Drug-Screen® FYL 10 Test?
The registered manufacturer of record for nal von minden Drug-Screen® FYL 10 Test is nal von minden GmbH.
What is the Primary UDI-DI identifier for nal von minden Drug-Screen® FYL 10 Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-nvm-101029Q4.
What classification code is assigned to this device?
This device is registered under product classification code W0102160508.
Similar Classification Devices (W0102160508)
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