MEDIU CLED (CLED AGAR) (UDI 05940540373408)
Manufactured by Sanimed International Impex S.A.
Device Regulatory Overview
The MEDIU CLED (CLED AGAR) (Model/Catalog Number: 22119) is a medical device manufactured by Sanimed International Impex S.A.. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 22119
- Product Code / EMDN
- W0104010405
- Device Name
- MEDIU CLED (CLED AGAR)
- Database Sync Date
- 2026-08-09 16:30:25
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MEDIU CLED (CLED AGAR)?
The registered manufacturer of record for MEDIU CLED (CLED AGAR) is Sanimed International Impex S.A..
What is the Primary UDI-DI identifier for MEDIU CLED (CLED AGAR)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540373408.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
Other Devices by Sanimed International Impex S.A.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint