eudamed_udi
Primary ID: 07331427270558
Kryckkäpp Flex lång, blå (UDI 07331427270558)
Manufactured by Swereco AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kryckkäpp Flex lång, blå - Primary ID 07331427270558
Device Regulatory Overview
The Kryckkäpp Flex lång, blå (Model/Catalog Number: 127055) is a medical device manufactured by Swereco AB. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 127055
- Product Code / EMDN
- Y12030601
- Device Name
- ELBOW CRUTCHES
- Database Sync Date
- 2026-08-09 16:29:27
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Kryckkäpp Flex lång, blå?
The registered manufacturer of record for Kryckkäpp Flex lång, blå is Swereco AB.
What is the Primary UDI-DI identifier for Kryckkäpp Flex lång, blå?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07331427270558.
What classification code is assigned to this device?
This device is registered under product classification code Y12030601.
Similar Classification Devices (Y12030601)
Other Devices by Swereco AB
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint