eudamed_udi
Primary ID: 00634782066420
Multikuf™ (UDI 00634782066420)
Manufactured by American Diagnostic Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Multikuf™ - Primary ID 00634782066420
Device Regulatory Overview
The Multikuf™ (Model/Catalog Number: 732-BK) is a medical device manufactured by American Diagnostic Corporation. This product is indexed under FDA Product Code / Category Classification C9006 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 732-BK
- Product Code / EMDN
- C9006
- Device Name
- Aneroid Sphygmomanometer
- Database Sync Date
- 2026-08-09 16:45:38
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 Multikuf™?
The registered manufacturer of record for Multikuf™ is American Diagnostic Corporation.
What is the Primary UDI-DI identifier for Multikuf™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00634782066420.
What classification code is assigned to this device?
This device is registered under product classification code C9006.
Similar Classification Devices (C9006)
Other Devices by American Diagnostic Corporation
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