eudamed_udi
Primary ID: 05419980256119
AQUAREL-1502 (UDI 05419980256119)
Manufactured by SIDENA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AQUAREL-1502 - Primary ID 05419980256119
Device Regulatory Overview
The AQUAREL-1502 (Model/Catalog Number: AQUAREL-1502) is a medical device manufactured by SIDENA. This product is indexed under FDA Product Code / Category Classification W0202059002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AQUAREL-1502
- Product Code / EMDN
- W0202059002
- Device Name
- AQUAREL-3P
- Database Sync Date
- 2026-08-09 16:50:12
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 AQUAREL-1502?
The registered manufacturer of record for AQUAREL-1502 is SIDENA.
What is the Primary UDI-DI identifier for AQUAREL-1502?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05419980256119.
What classification code is assigned to this device?
This device is registered under product classification code W0202059002.
Similar Classification Devices (W0202059002)
Other Devices by SIDENA
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