eudamed_udi
Primary ID: 05055788773269
Wystopper (UDI 05055788773269)
Manufactured by Flexicare Medical Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wystopper - Primary ID 05055788773269
Device Regulatory Overview
The Wystopper (Model/Catalog Number: WS0616) is a medical device manufactured by Flexicare Medical Limited. This product is indexed under FDA Product Code / Category Classification A108099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WS0616
- Product Code / EMDN
- A108099
- Device Name
- Stoma Plugs
- Database Sync Date
- 2026-08-09 16:29:26
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 Wystopper?
The registered manufacturer of record for Wystopper is Flexicare Medical Limited.
What is the Primary UDI-DI identifier for Wystopper?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05055788773269.
What classification code is assigned to this device?
This device is registered under product classification code A108099.
Similar Classification Devices (A108099)
Other Devices by Flexicare Medical Limited
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