eudamed_udi
Primary ID: 04250476600143
ORBIS (UDI 04250476600143)
Manufactured by Akzenta International SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ORBIS - Primary ID 04250476600143
Device Regulatory Overview
The ORBIS (Model/Catalog Number: 312417) is a medical device manufactured by Akzenta International SA. This product is indexed under FDA Product Code / Category Classification T0306 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 312417
- Product Code / EMDN
- T0306
- Device Name
- PATIENT TOWELS
- Database Sync Date
- 2026-08-09 16:45:49
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 ORBIS?
The registered manufacturer of record for ORBIS is Akzenta International SA.
What is the Primary UDI-DI identifier for ORBIS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250476600143.
What classification code is assigned to this device?
This device is registered under product classification code T0306.
Similar Classification Devices (T0306)
Other Devices by Akzenta International SA
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