CERVICOTHORACIC ORTHOSIS - MINERVA-L (UDI 08680853104906)
Manufactured by HEGELİ ORTOPEDİK ÜRÜNLER SAN.LTD.ŞTİ
Device Regulatory Overview
The CERVICOTHORACIC ORTHOSIS - MINERVA-L (Model/Catalog Number: ARN105-LRG) is a medical device manufactured by HEGELİ ORTOPEDİK ÜRÜNLER SAN.LTD.ŞTİ. This product is indexed under FDA Product Code / Category Classification Y060312 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ARN105-LRG
- Product Code / EMDN
- Y060312
- Device Name
- CERVICAL COLLARS
- Database Sync Date
- 2026-08-09 16:45:44
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 CERVICOTHORACIC ORTHOSIS - MINERVA-L?
The registered manufacturer of record for CERVICOTHORACIC ORTHOSIS - MINERVA-L is HEGELİ ORTOPEDİK ÜRÜNLER SAN.LTD.ŞTİ.
What is the Primary UDI-DI identifier for CERVICOTHORACIC ORTHOSIS - MINERVA-L?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680853104906.
What classification code is assigned to this device?
This device is registered under product classification code Y060312.
Similar Classification Devices (Y060312)
Other Devices by HEGELİ ORTOPEDİK ÜRÜNLER SAN.LTD.ŞTİ
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