gudid
Primary ID: 28941
SpeediCath Flex Set (UDI 28941)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SpeediCath Flex Set - Primary ID 28941
Device Regulatory Overview
The SpeediCath Flex Set (Model/Catalog Number: 28941) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification FCM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 28941
- Product Code / EMDN
- FCM
- Device Name
- Database Sync Date
- 2026-08-09 09:12:46
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 SpeediCath Flex Set?
The registered manufacturer of record for SpeediCath Flex Set is Coloplast A/S.
What is the Primary UDI-DI identifier for SpeediCath Flex Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28941.
What classification code is assigned to this device?
This device is registered under product classification code FCM.
Similar Classification Devices (FCM)
Other Devices by Coloplast A/S
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