GUDIDData
gudid Primary ID: NTPB201X

Wavelength (UDI NTPB201X)

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 NTPB201X

Device Regulatory Overview

The Wavelength (Model/Catalog Number: NTPB201X) 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
NTPB201X
Product Code / EMDN
MUI
Device Name
Wavelength LV Ultrasound Gel 8.45oz
Database Sync Date
2026-08-09 09:32:43

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

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 NTPB201X.

What classification code is assigned to this device?

This device is registered under product classification code MUI.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint