gudid
Primary ID: MN-150
EPSIMED (UDI MN-150)
Manufactured by EPSIMED LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EPSIMED - Primary ID MN-150
Device Regulatory Overview
The EPSIMED (Model/Catalog Number: MN-150) is a medical device manufactured by EPSIMED LLC. This product is indexed under FDA Product Code / Category Classification MWI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MN-150
- Product Code / EMDN
- MWI
- Device Name
- EPSIMEDMN-150PATIENT MONITOR
- Database Sync Date
- 2026-08-09 09:04:48
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 EPSIMED?
The registered manufacturer of record for EPSIMED is EPSIMED LLC.
What is the Primary UDI-DI identifier for EPSIMED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MN-150.
What classification code is assigned to this device?
This device is registered under product classification code MWI.
Similar Classification Devices (MWI)
Other Devices by EPSIMED LLC
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