eudamed_udi
Primary ID: 05907506237730
Medlance Plus, safety lancet (UDI 05907506237730)
Manufactured by HTL-Strefa S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medlance Plus, safety lancet - Primary ID 05907506237730
Device Regulatory Overview
The Medlance Plus, safety lancet (Model/Catalog Number: 7241) is a medical device manufactured by HTL-Strefa S.A.. This product is indexed under FDA Product Code / Category Classification V010401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7241
- Product Code / EMDN
- V010401
- Device Name
- Safety lancet
- Database Sync Date
- 2026-08-09 16:50:08
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 Medlance Plus, safety lancet?
The registered manufacturer of record for Medlance Plus, safety lancet is HTL-Strefa S.A..
What is the Primary UDI-DI identifier for Medlance Plus, safety lancet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907506237730.
What classification code is assigned to this device?
This device is registered under product classification code V010401.
Similar Classification Devices (V010401)
Other Devices by HTL-Strefa S.A.
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