MUELLER HINTON AGAR II 150 mm (UDI 08054187132308)
Manufactured by Biolife Italiana s.r.l.
Device Regulatory Overview
The MUELLER HINTON AGAR II 150 mm (Model/Catalog Number: 501740P) is a medical device manufactured by Biolife Italiana s.r.l.. This product is indexed under FDA Product Code / Category Classification W0104010403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 501740P
- Product Code / EMDN
- W0104010403
- Device Name
- MEDIAPLATES
- Database Sync Date
- 2026-08-09 17:30:19
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 MUELLER HINTON AGAR II 150 mm?
The registered manufacturer of record for MUELLER HINTON AGAR II 150 mm is Biolife Italiana s.r.l..
What is the Primary UDI-DI identifier for MUELLER HINTON AGAR II 150 mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08054187132308.
What classification code is assigned to this device?
This device is registered under product classification code W0104010403.
Similar Classification Devices (W0104010403)
Other Devices by Biolife Italiana s.r.l.
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