Cuff A3, black, 2 tubes large adult (UDI 04030155019516)
Manufactured by Kirchner & Wilhelm GmbH + Co KG
Device Regulatory Overview
The Cuff A3, black, 2 tubes large adult (Model/Catalog Number: 04.86600.241) is a medical device manufactured by Kirchner & Wilhelm GmbH + Co KG. This product is indexed under FDA Product Code / Category Classification C9006 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04.86600.241
- Product Code / EMDN
- C9006
- Device Name
- Aneroid sphygmomanometers
- 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 Cuff A3, black, 2 tubes large adult?
The registered manufacturer of record for Cuff A3, black, 2 tubes large adult is Kirchner & Wilhelm GmbH + Co KG.
What is the Primary UDI-DI identifier for Cuff A3, black, 2 tubes large adult?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04030155019516.
What classification code is assigned to this device?
This device is registered under product classification code C9006.
Similar Classification Devices (C9006)
Other Devices by Kirchner & Wilhelm GmbH + Co KG
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