Avalon ECG/IUP Transducer (UDI 00884838093201)
Manufactured by Philips Medizin Systeme Böblingen GmbH
Device Regulatory Overview
The Avalon ECG/IUP Transducer (Model/Catalog Number: 867247) is a medical device manufactured by Philips Medizin Systeme Böblingen GmbH. This product is indexed under FDA Product Code / Category Classification Z1208010499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 867247
- Product Code / EMDN
- Z1208010499
- Device Name
- Avalon ECG/IUP Transducer
- Database Sync Date
- 2026-08-09 16:46:14
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 Avalon ECG/IUP Transducer?
The registered manufacturer of record for Avalon ECG/IUP Transducer is Philips Medizin Systeme Böblingen GmbH.
What is the Primary UDI-DI identifier for Avalon ECG/IUP Transducer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838093201.
What classification code is assigned to this device?
This device is registered under product classification code Z1208010499.
Similar Classification Devices (Z1208010499)
Other Devices by Philips Medizin Systeme Böblingen GmbH
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