gudid
Primary ID: DW-230200
Saline Noze Mist (UDI DW-230200)
Manufactured by Dr. Noze Best, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Saline Noze Mist - Primary ID DW-230200
Device Regulatory Overview
The Saline Noze Mist (Model/Catalog Number: DW-230200) is a medical device manufactured by Dr. Noze Best, LLC. This product is indexed under FDA Product Code / Category Classification KCJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DW-230200
- Product Code / EMDN
- KCJ
- Device Name
- Saline nasal spray
- Database Sync Date
- 2026-08-09 09:37:44
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 Saline Noze Mist?
The registered manufacturer of record for Saline Noze Mist is Dr. Noze Best, LLC.
What is the Primary UDI-DI identifier for Saline Noze Mist?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DW-230200.
What classification code is assigned to this device?
This device is registered under product classification code KCJ.
Similar Classification Devices (KCJ)
Other Devices by Dr. Noze Best, LLC
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