eudamed_udi
Primary ID: 04063921000241
Heftpflaster (UDI 04063921000241)
Manufactured by Franz Kalff GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Heftpflaster - Primary ID 04063921000241
Device Regulatory Overview
The Heftpflaster (Model/Catalog Number: U07485) is a medical device manufactured by Franz Kalff GmbH. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- U07485
- Product Code / EMDN
- M050101
- Device Name
- Heftpflaster
- Database Sync Date
- 2026-08-09 16:28:48
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 Heftpflaster?
The registered manufacturer of record for Heftpflaster is Franz Kalff GmbH.
What is the Primary UDI-DI identifier for Heftpflaster?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04063921000241.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by Franz Kalff GmbH
Programmatic Export
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