gudid
Primary ID: CMS50D
CONTEC (UDI CMS50D)
Manufactured by BEURER NORTH AMERICA, L.P.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CONTEC - Primary ID CMS50D
Device Regulatory Overview
The CONTEC (Model/Catalog Number: CMS50D) is a medical device manufactured by BEURER NORTH AMERICA, L.P.. This product is indexed under FDA Product Code / Category Classification OCH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CMS50D
- Product Code / EMDN
- OCH
- Device Name
- Pulse Oximeter for use with sporting and aviation activities. Intended to monitor heart rate during exercise.
- Database Sync Date
- 2026-08-09 09:11:04
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 CONTEC?
The registered manufacturer of record for CONTEC is BEURER NORTH AMERICA, L.P..
What is the Primary UDI-DI identifier for CONTEC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CMS50D.
What classification code is assigned to this device?
This device is registered under product classification code OCH.
Similar Classification Devices (OCH)
Other Devices by BEURER NORTH AMERICA, L.P.
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