eudamed_udi
Primary ID: 05901549097092
Prolance (UDI 05901549097092)
Manufactured by HTL-Strefa S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Prolance - Primary ID 05901549097092
Device Regulatory Overview
The Prolance (Model/Catalog Number: 7620) 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
- 7620
- Product Code / EMDN
- V010401
- Device Name
- safety lancet
- Database Sync Date
- 2026-08-09 16:29:46
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 Prolance?
The registered manufacturer of record for Prolance is HTL-Strefa S.A..
What is the Primary UDI-DI identifier for Prolance?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901549097092.
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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