MEDIU CU LAURIL SULFAT DE SODIU (LAURYL SULPHATE BROTH) (UDI 05940540373460)
Manufactured by Sanimed International Impex S.A.
Device Regulatory Overview
The MEDIU CU LAURIL SULFAT DE SODIU (LAURYL SULPHATE BROTH) (Model/Catalog Number: 11448) is a medical device manufactured by Sanimed International Impex S.A.. This product is indexed under FDA Product Code / Category Classification W0104010306 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11448
- Product Code / EMDN
- W0104010306
- Device Name
- MEDIU CU LAURIL SULFAT DE SODIU (LAURYL SULPHATE BROTH)
- Database Sync Date
- 2026-08-09 16:50:27
Full Regulatory Attributes
🔒 Token Gated
{
"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 MEDIU CU LAURIL SULFAT DE SODIU (LAURYL SULPHATE BROTH)?
The registered manufacturer of record for MEDIU CU LAURIL SULFAT DE SODIU (LAURYL SULPHATE BROTH) is Sanimed International Impex S.A..
What is the Primary UDI-DI identifier for MEDIU CU LAURIL SULFAT DE SODIU (LAURYL SULPHATE BROTH)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540373460.
What classification code is assigned to this device?
This device is registered under product classification code W0104010306.
Similar Classification Devices (W0104010306)
Other Devices by Sanimed International Impex S.A.
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