eudamed_udi
Primary ID: 04251778101710
Detall (UDI 04251778101710)
Manufactured by HÄLSA Pharma GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Detall - Primary ID 04251778101710
Device Regulatory Overview
The Detall (Model/Catalog Number: 100001) is a medical device manufactured by HÄLSA Pharma GmbH. This product is indexed under FDA Product Code / Category Classification A13 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100001
- Product Code / EMDN
- A13
- Device Name
- Detall
- Database Sync Date
- 2026-08-09 16:45:03
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 Detall?
The registered manufacturer of record for Detall is HÄLSA Pharma GmbH.
What is the Primary UDI-DI identifier for Detall?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251778101710.
What classification code is assigned to this device?
This device is registered under product classification code A13.
Similar Classification Devices (A13)
Other Devices by HÄLSA Pharma GmbH
Programmatic Export
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JSON API Endpoint