eudamed_udi
Primary ID: 09010727001144
Wellion LANCETS (UDI 09010727001144)
Manufactured by MED TRUST Handelsges.m.b.H.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wellion LANCETS - Primary ID 09010727001144
Device Regulatory Overview
The Wellion LANCETS (Model/Catalog Number: WELL203R) is a medical device manufactured by MED TRUST Handelsges.m.b.H.. This product is indexed under FDA Product Code / Category Classification V010402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WELL203R
- Product Code / EMDN
- V010402
- Device Name
- Wellion LANCETS
- Database Sync Date
- 2026-08-09 16:29:38
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 Wellion LANCETS?
The registered manufacturer of record for Wellion LANCETS is MED TRUST Handelsges.m.b.H..
What is the Primary UDI-DI identifier for Wellion LANCETS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09010727001144.
What classification code is assigned to this device?
This device is registered under product classification code V010402.
Similar Classification Devices (V010402)
Other Devices by MED TRUST Handelsges.m.b.H.
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