gudid
Primary ID: 9033S0581
Keypoint (UDI 9033S0581)
Manufactured by NATUS MANUFACTURING LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Keypoint - Primary ID 9033S0581
Device Regulatory Overview
The Keypoint (Model/Catalog Number: 9033S0581) is a medical device manufactured by NATUS MANUFACTURING LIMITED. This product is indexed under FDA Product Code / Category Classification GWF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9033S0581
- Product Code / EMDN
- GWF
- Device Name
- Single Fiber EMG
- Database Sync Date
- 2026-08-09 10:02:47
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 Keypoint?
The registered manufacturer of record for Keypoint is NATUS MANUFACTURING LIMITED.
What is the Primary UDI-DI identifier for Keypoint?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9033S0581.
What classification code is assigned to this device?
This device is registered under product classification code GWF.
Similar Classification Devices (GWF)
Other Devices by NATUS MANUFACTURING LIMITED
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