eudamed_udi
Primary ID: 03597610613005
ANIOSYME X3 (UDI 03597610613005)
Manufactured by Laboratoires Anios
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ANIOSYME X3 - Primary ID 03597610613005
Device Regulatory Overview
The ANIOSYME X3 (Model/Catalog Number: 26330386D) is a medical device manufactured by Laboratoires Anios. This product is indexed under FDA Product Code / Category Classification D0901 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 26330386D
- Product Code / EMDN
- D0901
- Device Name
- ANIOSYME X3 2X5L
- Database Sync Date
- 2026-08-09 16:28:58
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 ANIOSYME X3?
The registered manufacturer of record for ANIOSYME X3 is Laboratoires Anios.
What is the Primary UDI-DI identifier for ANIOSYME X3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610613005.
What classification code is assigned to this device?
This device is registered under product classification code D0901.
Similar Classification Devices (D0901)
Other Devices by Laboratoires Anios
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