eudamed_udi
Primary ID: 08426521421254
MenaLancet (UDI 08426521421254)
Manufactured by HTL-Strefa S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MenaLancet - Primary ID 08426521421254
Device Regulatory Overview
The MenaLancet (Model/Catalog Number: 7152) is a medical device manufactured by HTL-Strefa S.A.. This product is indexed under FDA Product Code / Category Classification V010402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7152
- Product Code / EMDN
- V010402
- Device Name
- Personal lancet
- Database Sync Date
- 2026-08-09 16:44:58
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 MenaLancet?
The registered manufacturer of record for MenaLancet is HTL-Strefa S.A..
What is the Primary UDI-DI identifier for MenaLancet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08426521421254.
What classification code is assigned to this device?
This device is registered under product classification code V010402.
Similar Classification Devices (V010402)
Other Devices by HTL-Strefa S.A.
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