eudamed_udi
Primary ID: 08051084181156
SONICA (UDI 08051084181156)
Manufactured by SOLTEC S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SONICA - Primary ID 08051084181156
Device Regulatory Overview
The SONICA (Model/Catalog Number: 4200 M S3 SO V2) is a medical device manufactured by SOLTEC S.r.l.. This product is indexed under FDA Product Code / Category Classification Z12011302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4200 M S3 SO V2
- Product Code / EMDN
- Z12011302
- Device Name
- ULTRASONIC CLEANER
- Database Sync Date
- 2026-08-09 16:30:29
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 SONICA?
The registered manufacturer of record for SONICA is SOLTEC S.r.l..
What is the Primary UDI-DI identifier for SONICA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051084181156.
What classification code is assigned to this device?
This device is registered under product classification code Z12011302.
Similar Classification Devices (Z12011302)
Other Devices by SOLTEC S.r.l.
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