eudamed_udi
Primary ID: 05745000569113
Careturner - Vendesystem til OPUS 7 (UDI 05745000569113)
Manufactured by Careturner A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Careturner - Vendesystem til OPUS 7 - Primary ID 05745000569113
Device Regulatory Overview
The Careturner - Vendesystem til OPUS 7 (Model/Catalog Number: ABLOPUS7200821) is a medical device manufactured by Careturner A/S. This product is indexed under FDA Product Code / Category Classification V08068099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ABLOPUS7200821
- Product Code / EMDN
- V08068099
- Device Name
- Careturner
- 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 Careturner - Vendesystem til OPUS 7?
The registered manufacturer of record for Careturner - Vendesystem til OPUS 7 is Careturner A/S.
What is the Primary UDI-DI identifier for Careturner - Vendesystem til OPUS 7?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05745000569113.
What classification code is assigned to this device?
This device is registered under product classification code V08068099.
Similar Classification Devices (V08068099)
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