Περικάρπιο με Δέστρα Neoprene Medium (UDI 05205414040023)
Manufactured by ADCO ORTHOPAEDICS LTD
Device Regulatory Overview
The Περικάρπιο με Δέστρα Neoprene Medium (Model/Catalog Number: 03204) is a medical device manufactured by ADCO ORTHOPAEDICS LTD. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03204
- Product Code / EMDN
- Y060612
- Device Name
- Περικάρπιο με Δέστρα Neoprene
- Database Sync Date
- 2026-08-09 16:29:04
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 Περικάρπιο με Δέστρα Neoprene Medium?
The registered manufacturer of record for Περικάρπιο με Δέστρα Neoprene Medium is ADCO ORTHOPAEDICS LTD.
What is the Primary UDI-DI identifier for Περικάρπιο με Δέστρα Neoprene Medium?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05205414040023.
What classification code is assigned to this device?
This device is registered under product classification code Y060612.
Similar Classification Devices (Y060612)
Other Devices by ADCO ORTHOPAEDICS LTD
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