eudamed_udi
Primary ID: 07330945819515
Selection Ulnar Deviation (UDI 07330945819515)
Manufactured by Camp Scandinavia AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Selection Ulnar Deviation - Primary ID 07330945819515
Device Regulatory Overview
The Selection Ulnar Deviation (Model/Catalog Number: 352181010) is a medical device manufactured by Camp Scandinavia AB. This product is indexed under FDA Product Code / Category Classification Y060603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 352181010
- Product Code / EMDN
- Y060603
- Device Name
- Selection Ulnar Deviation
- Database Sync Date
- 2026-08-09 16:29:08
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 Selection Ulnar Deviation?
The registered manufacturer of record for Selection Ulnar Deviation is Camp Scandinavia AB.
What is the Primary UDI-DI identifier for Selection Ulnar Deviation?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07330945819515.
What classification code is assigned to this device?
This device is registered under product classification code Y060603.
Similar Classification Devices (Y060603)
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