BONA Mulltupfer 6 G haselnuss (UDI EWWV002478351)
Manufactured by Wilhelm Weisweiler GmbH & Co. KG
Device Regulatory Overview
The BONA Mulltupfer 6 G haselnuss (Model/Catalog Number: 00247835) is a medical device manufactured by Wilhelm Weisweiler GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification M020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00247835
- Product Code / EMDN
- M020199
- Device Name
- BONA Mulltupfer 3 P linse
- Database Sync Date
- 2026-08-09 16:49:26
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 BONA Mulltupfer 6 G haselnuss?
The registered manufacturer of record for BONA Mulltupfer 6 G haselnuss is Wilhelm Weisweiler GmbH & Co. KG.
What is the Primary UDI-DI identifier for BONA Mulltupfer 6 G haselnuss?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EWWV002478351.
What classification code is assigned to this device?
This device is registered under product classification code M020199.
Similar Classification Devices (M020199)
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