eudamed_udi
Primary ID: 04251778103882
EspiForte (UDI 04251778103882)
Manufactured by HÄLSA Pharma GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EspiForte - Primary ID 04251778103882
Device Regulatory Overview
The EspiForte (Model/Catalog Number: CATA-MD301-00000) is a medical device manufactured by HÄLSA Pharma GmbH. This product is indexed under FDA Product Code / Category Classification G0401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CATA-MD301-00000
- Product Code / EMDN
- G0401
- Device Name
- Simeticone Capsules
- Database Sync Date
- 2026-08-09 16:30:25
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 EspiForte?
The registered manufacturer of record for EspiForte is HÄLSA Pharma GmbH.
What is the Primary UDI-DI identifier for EspiForte?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251778103882.
What classification code is assigned to this device?
This device is registered under product classification code G0401.
Similar Classification Devices (G0401)
Other Devices by HÄLSA Pharma GmbH
Programmatic Export
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