eudamed_udi
Primary ID: +M582NEMCA1340
NEMCA134 (UDI +M582NEMCA1340)
Manufactured by NorthEast Monitoring, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NEMCA134 - Primary ID +M582NEMCA1340
Device Regulatory Overview
The NEMCA134 (Model/Catalog Number: NEMCA134) is a medical device manufactured by NorthEast Monitoring, Inc.. This product is indexed under FDA Product Code / Category Classification Z12030680 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NEMCA134
- Product Code / EMDN
- Z12030680
- Device Name
- DR200 patient cable
- Database Sync Date
- 2026-08-09 17:57:30
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 NEMCA134?
The registered manufacturer of record for NEMCA134 is NorthEast Monitoring, Inc..
What is the Primary UDI-DI identifier for NEMCA134?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +M582NEMCA1340.
What classification code is assigned to this device?
This device is registered under product classification code Z12030680.
Similar Classification Devices (Z12030680)
Other Devices by NorthEast Monitoring, Inc.
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