eudamed_udi
Primary ID: 00841517110239
Sonosite PX (UDI 00841517110239)
Manufactured by Fujifilm Sonosite, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sonosite PX - Primary ID 00841517110239
Device Regulatory Overview
The Sonosite PX (Model/Catalog Number: P33206-01) is a medical device manufactured by Fujifilm Sonosite, Inc.. This product is indexed under FDA Product Code / Category Classification Z1104018099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P33206-01
- Product Code / EMDN
- Z1104018099
- Device Name
- SONOSITE MICROPHONE ACCESSORY
- Database Sync Date
- 2026-08-09 16:28:46
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 Sonosite PX?
The registered manufacturer of record for Sonosite PX is Fujifilm Sonosite, Inc..
What is the Primary UDI-DI identifier for Sonosite PX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00841517110239.
What classification code is assigned to this device?
This device is registered under product classification code Z1104018099.
Similar Classification Devices (Z1104018099)
Other Devices by Fujifilm Sonosite, Inc.
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