gudid
Primary ID: 108210
Nomoline (UDI 108210)
Manufactured by MASIMO CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nomoline - Primary ID 108210
Device Regulatory Overview
The Nomoline (Model/Catalog Number: 108210) is a medical device manufactured by MASIMO CORPORATION. This product is indexed under FDA Product Code / Category Classification CCK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 108210
- Product Code / EMDN
- CCK
- Device Name
- Database Sync Date
- 2026-08-09 09:21:51
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 Nomoline?
The registered manufacturer of record for Nomoline is MASIMO CORPORATION.
What is the Primary UDI-DI identifier for Nomoline?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 108210.
What classification code is assigned to this device?
This device is registered under product classification code CCK.
Similar Classification Devices (CCK)
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