eudamed_udi
Primary ID: 05205414004421
Καλσόν ClassI ΚΔ Μαύρο XXLarge (UDI 05205414004421)
Manufactured by ADCO ORTHOPAEDICS LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Καλσόν ClassI ΚΔ Μαύρο XXLarge - Primary ID 05205414004421
Device Regulatory Overview
The Καλσόν ClassI ΚΔ Μαύρο XXLarge (Model/Catalog Number: 07180) is a medical device manufactured by ADCO ORTHOPAEDICS LTD. This product is indexed under FDA Product Code / Category Classification M030405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 07180
- Product Code / EMDN
- M030405
- Device Name
- Καλσόν ClassI ΚΔ
- Database Sync Date
- 2026-08-09 16:28:46
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 Καλσόν ClassI ΚΔ Μαύρο XXLarge?
The registered manufacturer of record for Καλσόν ClassI ΚΔ Μαύρο XXLarge is ADCO ORTHOPAEDICS LTD.
What is the Primary UDI-DI identifier for Καλσόν ClassI ΚΔ Μαύρο XXLarge?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05205414004421.
What classification code is assigned to this device?
This device is registered under product classification code M030405.
Similar Classification Devices (M030405)
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