gudid
Primary ID: ELECTRODE SOLUTION AND SKIN PREP
SIGNASPRAY (UDI ELECTRODE SOLUTION AND SKIN PREP)
Manufactured by PARKER LABORATORIES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SIGNASPRAY - Primary ID ELECTRODE SOLUTION AND SKIN PREP
Device Regulatory Overview
The SIGNASPRAY (Model/Catalog Number: ELECTRODE SOLUTION AND SKIN PREP) 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
- ELECTRODE SOLUTION AND SKIN PREP
- Product Code / EMDN
- GYB
- Device Name
- Signaspray Electrode Solution and Skin Prep, 250 ml bottle
- Database Sync Date
- 2026-08-09 09:49:29
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 SIGNASPRAY?
The registered manufacturer of record for SIGNASPRAY is PARKER LABORATORIES INC.
What is the Primary UDI-DI identifier for SIGNASPRAY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ELECTRODE SOLUTION AND SKIN PREP.
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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