gudid
Primary ID: 9590 BLUE, OXIMETER
FINGERTIP PULSE OXIMETER (UDI 9590 BLUE, OXIMETER)
Manufactured by NONIN MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FINGERTIP PULSE OXIMETER - Primary ID 9590 BLUE, OXIMETER
Device Regulatory Overview
The FINGERTIP PULSE OXIMETER (Model/Catalog Number: 9590 BLUE, OXIMETER) is a medical device manufactured by NONIN MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification DQA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9590 BLUE, OXIMETER
- Product Code / EMDN
- DQA
- Device Name
- FINGERTIP PULSE OXIMETER with 9590 BLUE, OXIMETER
- Database Sync Date
- 2026-08-09 09:33:17
Full Regulatory Attributes
🔒 Token Gated
{
"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 FINGERTIP PULSE OXIMETER?
The registered manufacturer of record for FINGERTIP PULSE OXIMETER is NONIN MEDICAL, INC..
What is the Primary UDI-DI identifier for FINGERTIP PULSE OXIMETER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9590 BLUE, OXIMETER.
What classification code is assigned to this device?
This device is registered under product classification code DQA.
Similar Classification Devices (DQA)
Other Devices by NONIN MEDICAL, INC.
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