MEDIU HUGH-LEIFSON (HUGH LEIFSON GLUCOSE MEDIUM) (UDI 05940540370919)
Manufactured by Sanimed International Impex S.A.
Device Regulatory Overview
The MEDIU HUGH-LEIFSON (HUGH LEIFSON GLUCOSE MEDIUM) (Model/Catalog Number: 31601) is a medical device manufactured by Sanimed International Impex S.A.. This product is indexed under FDA Product Code / Category Classification W0104010206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 31601
- Product Code / EMDN
- W0104010206
- Device Name
- MEDIU HUGH-LEIFSON (HUGH LEIFSON GLUCOSE MEDIUM)
- Database Sync Date
- 2026-08-09 16:48:36
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 MEDIU HUGH-LEIFSON (HUGH LEIFSON GLUCOSE MEDIUM)?
The registered manufacturer of record for MEDIU HUGH-LEIFSON (HUGH LEIFSON GLUCOSE MEDIUM) is Sanimed International Impex S.A..
What is the Primary UDI-DI identifier for MEDIU HUGH-LEIFSON (HUGH LEIFSON GLUCOSE MEDIUM)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540370919.
What classification code is assigned to this device?
This device is registered under product classification code W0104010206.
Similar Classification Devices (W0104010206)
Other Devices by Sanimed International Impex S.A.
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