eudamed_udi
Primary ID: 05903999601577
diamet, mySafety (UDI 05903999601577)
Manufactured by HTL-Strefa S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for diamet, mySafety - Primary ID 05903999601577
Device Regulatory Overview
The diamet, mySafety (Model/Catalog Number: 7488) 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
- 7488
- Product Code / EMDN
- V010401
- Device Name
- safety lancet
- Database Sync Date
- 2026-08-09 16:51:37
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 diamet, mySafety?
The registered manufacturer of record for diamet, mySafety is HTL-Strefa S.A..
What is the Primary UDI-DI identifier for diamet, mySafety?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903999601577.
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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