eudamed_udi
Primary ID: 05907506237945
Haemolance Plus (UDI 05907506237945)
Manufactured by HTL-Strefa S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Haemolance Plus - Primary ID 05907506237945
Device Regulatory Overview
The Haemolance Plus (Model/Catalog Number: 7367) 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
- 7367
- Product Code / EMDN
- V010401
- Device Name
- safety lancet
- Database Sync Date
- 2026-08-09 16:45:00
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 Haemolance Plus?
The registered manufacturer of record for Haemolance Plus is HTL-Strefa S.A..
What is the Primary UDI-DI identifier for Haemolance Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907506237945.
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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