gudid
Primary ID: NTPF900X
Wavelength (UDI NTPF900X)
Manufactured by National Therapy Products Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wavelength - Primary ID NTPF900X
Device Regulatory Overview
The Wavelength (Model/Catalog Number: NTPF900X) is a medical device manufactured by National Therapy Products Inc. This product is indexed under FDA Product Code / Category Classification MUI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NTPF900X
- Product Code / EMDN
- MUI
- Device Name
- Wavelength HV Transmission Gel 210L
- Database Sync Date
- 2026-08-09 09:32:43
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 Wavelength?
The registered manufacturer of record for Wavelength is National Therapy Products Inc.
What is the Primary UDI-DI identifier for Wavelength?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NTPF900X.
What classification code is assigned to this device?
This device is registered under product classification code MUI.
Similar Classification Devices (MUI)
Other Devices by National Therapy Products Inc
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