SONOREX SUPER RK 1040 (UDI +EBAN3190Q)
Manufactured by BANDELIN electronic GmbH & Co. KG
Device Regulatory Overview
The SONOREX SUPER RK 1040 (Model/Catalog Number: 319) is a medical device manufactured by BANDELIN electronic GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Z12011302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 319
- Product Code / EMDN
- Z12011302
- Device Name
- SONOREX High-performance ultrasonic baths
- Database Sync Date
- 2026-08-09 16:46:24
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 SONOREX SUPER RK 1040?
The registered manufacturer of record for SONOREX SUPER RK 1040 is BANDELIN electronic GmbH & Co. KG.
What is the Primary UDI-DI identifier for SONOREX SUPER RK 1040?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +EBAN3190Q.
What classification code is assigned to this device?
This device is registered under product classification code Z12011302.
Similar Classification Devices (Z12011302)
Other Devices by BANDELIN electronic GmbH & Co. KG
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