gudid
Primary ID: 23-205
PHOENIX DIAGNOSTICS, INC. (UDI 23-205)
Manufactured by PHOENIX DIAGNOSTICS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PHOENIX DIAGNOSTICS, INC. - Primary ID 23-205
Device Regulatory Overview
The PHOENIX DIAGNOSTICS, INC. (Model/Catalog Number: 23-205) is a medical device manufactured by PHOENIX DIAGNOSTICS, INC.. This product is indexed under FDA Product Code / Category Classification JCB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 23-205
- Product Code / EMDN
- JCB
- Device Name
- Acid Wash for Tokyo Boeki BiOLiS 50i Series Electrolyte Systems
- Database Sync Date
- 2026-08-09 09:49:32
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 PHOENIX DIAGNOSTICS, INC.?
The registered manufacturer of record for PHOENIX DIAGNOSTICS, INC. is PHOENIX DIAGNOSTICS, INC..
What is the Primary UDI-DI identifier for PHOENIX DIAGNOSTICS, INC.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 23-205.
What classification code is assigned to this device?
This device is registered under product classification code JCB.
Similar Classification Devices (JCB)
Other Devices by PHOENIX DIAGNOSTICS, INC.
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