GUDIDData
eudamed_udi Primary ID: D-nvm-101009PW

nal von minden Drug-Screen® MOR/OPI 300 Test (UDI D-nvm-101009PW)

Manufactured by nal von minden GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for nal von minden Drug-Screen® MOR/OPI 300 Test - Primary ID D-nvm-101009PW

Device Regulatory Overview

The nal von minden Drug-Screen® MOR/OPI 300 Test (Model/Catalog Number: 101009) 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
101009
Product Code / EMDN
W0102160508
Device Name
MOR/OPI 300 Test
Database Sync Date
2026-08-09 17:57:54

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of nal von minden Drug-Screen® MOR/OPI 300 Test?

The registered manufacturer of record for nal von minden Drug-Screen® MOR/OPI 300 Test is nal von minden GmbH.

What is the Primary UDI-DI identifier for nal von minden Drug-Screen® MOR/OPI 300 Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-nvm-101009PW.

What classification code is assigned to this device?

This device is registered under product classification code W0102160508.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint