gudid
Primary ID: ELECTROLYTE CREME
REDUX (UDI ELECTROLYTE CREME)
Manufactured by PARKER LABORATORIES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for REDUX - Primary ID ELECTROLYTE CREME
Device Regulatory Overview
The REDUX (Model/Catalog Number: ELECTROLYTE CREME) is a medical device manufactured by PARKER LABORATORIES INC. This product is indexed under FDA Product Code / Category Classification GYB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ELECTROLYTE CREME
- Product Code / EMDN
- GYB
- Device Name
- Redux Electrolyte Crme, 4 oz. Tube
- Database Sync Date
- 2026-08-09 09:58:58
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 REDUX?
The registered manufacturer of record for REDUX is PARKER LABORATORIES INC.
What is the Primary UDI-DI identifier for REDUX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ELECTROLYTE CREME.
What classification code is assigned to this device?
This device is registered under product classification code GYB.
Similar Classification Devices (GYB)
Other Devices by PARKER LABORATORIES INC
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