eudamed_udi
Primary ID: D-nvm-103071S-25UE
MultiDip 7-3X Test (UDI D-nvm-103071S-25UE)
Manufactured by nal von minden GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MultiDip 7-3X Test - Primary ID D-nvm-103071S-25UE
Device Regulatory Overview
The MultiDip 7-3X Test (Model/Catalog Number: 103071S-25) is a medical device manufactured by nal von minden GmbH. This product is indexed under FDA Product Code / Category Classification W0102160511 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 103071S-25
- Product Code / EMDN
- W0102160511
- Device Name
- MultiDip 7-3X Test
- Database Sync Date
- 2026-08-09 16:29:09
Full Regulatory Attributes
đź”’ Token Gated
{
"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 MultiDip 7-3X Test?
The registered manufacturer of record for MultiDip 7-3X Test is nal von minden GmbH.
What is the Primary UDI-DI identifier for MultiDip 7-3X Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-nvm-103071S-25UE.
What classification code is assigned to this device?
This device is registered under product classification code W0102160511.
Similar Classification Devices (W0102160511)
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