eudamed_udi
Primary ID: 04049500983921
Pruban (UDI 04049500983921)
Manufactured by HARTMANN - RICO a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pruban - Primary ID 04049500983921
Device Regulatory Overview
The Pruban (Model/Catalog Number: 427314) is a medical device manufactured by HARTMANN - RICO a.s.. This product is indexed under FDA Product Code / Category Classification M03030103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 427314
- Product Code / EMDN
- M03030103
- Device Name
- Pruban
- Database Sync Date
- 2026-08-09 16:29:10
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 Pruban?
The registered manufacturer of record for Pruban is HARTMANN - RICO a.s..
What is the Primary UDI-DI identifier for Pruban?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049500983921.
What classification code is assigned to this device?
This device is registered under product classification code M03030103.
Similar Classification Devices (M03030103)
Other Devices by HARTMANN - RICO a.s.
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