eudamed_udi
Primary ID: 05016003585203
Single-Let (UDI 05016003585203)
Manufactured by HTL-Strefa S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Single-Let - Primary ID 05016003585203
Device Regulatory Overview
The Single-Let (Model/Catalog Number: 9036) 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
- 9036
- Product Code / EMDN
- V010401
- Device Name
- safety lancet
- Database Sync Date
- 2026-08-09 16:49:40
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 Single-Let?
The registered manufacturer of record for Single-Let is HTL-Strefa S.A..
What is the Primary UDI-DI identifier for Single-Let?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05016003585203.
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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