eudamed_udi
Primary ID: 05709817555417
Dansac (UDI 05709817555417)
Manufactured by Dansac A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dansac - Primary ID 05709817555417
Device Regulatory Overview
The Dansac (Model/Catalog Number: 932-20) is a medical device manufactured by Dansac A/S. This product is indexed under FDA Product Code / Category Classification A1001010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 932-20
- Product Code / EMDN
- A1001010202
- Device Name
- 1-Piece Closed Ostomy Pouch, GX, Convex
- Database Sync Date
- 2026-08-09 16:28:48
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 Dansac?
The registered manufacturer of record for Dansac is Dansac A/S.
What is the Primary UDI-DI identifier for Dansac?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05709817555417.
What classification code is assigned to this device?
This device is registered under product classification code A1001010202.
Similar Classification Devices (A1001010202)
Other Devices by Dansac A/S
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