eudamed_udi
Primary ID: 110755502084
Holzmundspatel, einzeln verpackt, 100 Stk (UDI 110755502084)
Manufactured by Büttner-Frank GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Holzmundspatel, einzeln verpackt, 100 Stk - Primary ID 110755502084
Device Regulatory Overview
The Holzmundspatel, einzeln verpackt, 100 Stk (Model/Catalog Number: 102868) is a medical device manufactured by Büttner-Frank GmbH. This product is indexed under FDA Product Code / Category Classification V9001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 102868
- Product Code / EMDN
- V9001
- Device Name
- Holzmundspatel
- Database Sync Date
- 2026-08-09 16:50:31
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 Holzmundspatel, einzeln verpackt, 100 Stk?
The registered manufacturer of record for Holzmundspatel, einzeln verpackt, 100 Stk is Büttner-Frank GmbH.
What is the Primary UDI-DI identifier for Holzmundspatel, einzeln verpackt, 100 Stk?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 110755502084.
What classification code is assigned to this device?
This device is registered under product classification code V9001.
Similar Classification Devices (V9001)
Other Devices by Büttner-Frank GmbH
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