gudid
Primary ID: EMO-100
EMAY (UDI EMO-100)
Manufactured by EMAY (HK) LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EMAY - Primary ID EMO-100
Device Regulatory Overview
The EMAY (Model/Catalog Number: EMO-100) is a medical device manufactured by EMAY (HK) LIMITED. This product is indexed under FDA Product Code / Category Classification OCH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EMO-100
- Product Code / EMDN
- OCH
- Device Name
- The Fingertip Pulse Oximeter is non-invasive device intended for spotchecking of functional oxygen saturation of arterial hemoglobin (Spo2) and pulse rate.
- Database Sync Date
- 2026-08-09 09:46:04
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 EMAY?
The registered manufacturer of record for EMAY is EMAY (HK) LIMITED.
What is the Primary UDI-DI identifier for EMAY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EMO-100.
What classification code is assigned to this device?
This device is registered under product classification code OCH.
Similar Classification Devices (OCH)
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