gudid
Primary ID: 02-0305
EASYMIX pro (UDI 02-0305)
Manufactured by OSARTIS GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EASYMIX pro - Primary ID 02-0305
Device Regulatory Overview
The EASYMIX pro (Model/Catalog Number: 02-0305) is a medical device manufactured by OSARTIS GmbH. This product is indexed under FDA Product Code / Category Classification JDZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02-0305
- Product Code / EMDN
- JDZ
- Device Name
- Vacuum mixing system for mixing of PMMA bone cements
- Database Sync Date
- 2026-08-09 09:17:36
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 EASYMIX pro?
The registered manufacturer of record for EASYMIX pro is OSARTIS GmbH.
What is the Primary UDI-DI identifier for EASYMIX pro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 02-0305.
What classification code is assigned to this device?
This device is registered under product classification code JDZ.
Similar Classification Devices (JDZ)
Other Devices by OSARTIS GmbH
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