eudamed_udi
Primary ID: 03665965000136
Atalante X (UDI 03665965000136)
Manufactured by Wandercraft
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Atalante X - Primary ID 03665965000136
Device Regulatory Overview
The Atalante X (Model/Catalog Number: ATA-002-IT) is a medical device manufactured by Wandercraft. This product is indexed under FDA Product Code / Category Classification Y061218 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ATA-002-IT
- Product Code / EMDN
- Y061218
- Device Name
- Atalante X
- Database Sync Date
- 2026-08-09 16:29:36
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 Atalante X?
The registered manufacturer of record for Atalante X is Wandercraft.
What is the Primary UDI-DI identifier for Atalante X?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03665965000136.
What classification code is assigned to this device?
This device is registered under product classification code Y061218.
Similar Classification Devices (Y061218)
Other Devices by Wandercraft
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