eudamed_udi
Primary ID: 05903999608118
droplet (UDI 05903999608118)
Manufactured by HTL-Strefa S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for droplet - Primary ID 05903999608118
Device Regulatory Overview
The droplet (Model/Catalog Number: 4114) is a medical device manufactured by HTL-Strefa S.A.. This product is indexed under FDA Product Code / Category Classification A0101010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4114
- Product Code / EMDN
- A0101010202
- Device Name
- Pen needle
- Database Sync Date
- 2026-08-09 16:50:57
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 droplet?
The registered manufacturer of record for droplet is HTL-Strefa S.A..
What is the Primary UDI-DI identifier for droplet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903999608118.
What classification code is assigned to this device?
This device is registered under product classification code A0101010202.
Similar Classification Devices (A0101010202)
Other Devices by HTL-Strefa S.A.
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