eudamed_udi
Primary ID: D-7384BX
MyStar SylkFeel (UDI D-7384BX)
Manufactured by HTL-Strefa S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MyStar SylkFeel - Primary ID D-7384BX
Device Regulatory Overview
The MyStar SylkFeel (Model/Catalog Number: 7384) 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
- 7384
- Product Code / EMDN
- V010402
- Device Name
- personal lancet
- Database Sync Date
- 2026-08-09 16:49:18
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 MyStar SylkFeel?
The registered manufacturer of record for MyStar SylkFeel is HTL-Strefa S.A..
What is the Primary UDI-DI identifier for MyStar SylkFeel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-7384BX.
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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