gudid
Primary ID: USB310
Oscilla (UDI USB310)
Manufactured by Inmedico A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Oscilla - Primary ID USB310
Device Regulatory Overview
The Oscilla (Model/Catalog Number: USB310) is a medical device manufactured by Inmedico A/S. This product is indexed under FDA Product Code / Category Classification EWO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- USB310
- Product Code / EMDN
- EWO
- Device Name
- Database Sync Date
- 2026-08-09 09:12:40
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 Oscilla?
The registered manufacturer of record for Oscilla is Inmedico A/S.
What is the Primary UDI-DI identifier for Oscilla?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is USB310.
What classification code is assigned to this device?
This device is registered under product classification code EWO.
Similar Classification Devices (EWO)
Other Devices by Inmedico A/S
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