ORX CO 820 ÇİFT / ORX CO 820 DOUBLE CHILD INGUINAL LIGAMENT DOUBLE (UDI 08682132206080)
Manufactured by EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ
Device Regulatory Overview
The ORX CO 820 ÇİFT / ORX CO 820 DOUBLE CHILD INGUINAL LIGAMENT DOUBLE (Model/Catalog Number: ORX CO 820 ÇİFT) is a medical device manufactured by EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ. This product is indexed under FDA Product Code / Category Classification Y060499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ORX CO 820 ÇİFT
- Product Code / EMDN
- Y060499
- Device Name
- CORSET SUPPORTS
- Database Sync Date
- 2026-08-09 16:44:59
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 ORX CO 820 ÇİFT / ORX CO 820 DOUBLE CHILD INGUINAL LIGAMENT DOUBLE?
The registered manufacturer of record for ORX CO 820 ÇİFT / ORX CO 820 DOUBLE CHILD INGUINAL LIGAMENT DOUBLE is EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ.
What is the Primary UDI-DI identifier for ORX CO 820 ÇİFT / ORX CO 820 DOUBLE CHILD INGUINAL LIGAMENT DOUBLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682132206080.
What classification code is assigned to this device?
This device is registered under product classification code Y060499.
Similar Classification Devices (Y060499)
Other Devices by EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ
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