gudid
Primary ID: 21600
Zewa (UDI 21600)
Manufactured by VERIDIAN HEALTHCARE LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Zewa - Primary ID 21600
Device Regulatory Overview
The Zewa (Model/Catalog Number: 21600) is a medical device manufactured by VERIDIAN HEALTHCARE LLC. This product is indexed under FDA Product Code / Category Classification PGJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21600
- Product Code / EMDN
- PGJ
- Device Name
- Pulse Ox OTC
- Database Sync Date
- 2026-08-09 09:17:18
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 Zewa?
The registered manufacturer of record for Zewa is VERIDIAN HEALTHCARE LLC.
What is the Primary UDI-DI identifier for Zewa?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 21600.
What classification code is assigned to this device?
This device is registered under product classification code PGJ.
Similar Classification Devices (PGJ)
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