gudid
Primary ID: ELECTRODE GEL
SIGNAGEL (UDI ELECTRODE GEL)
Manufactured by PARKER LABORATORIES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SIGNAGEL - Primary ID ELECTRODE GEL
Device Regulatory Overview
The SIGNAGEL (Model/Catalog Number: ELECTRODE GEL) 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 GEL
- Product Code / EMDN
- GYB
- Device Name
- Signagel Electrode Gel, 250 gram 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 SIGNAGEL?
The registered manufacturer of record for SIGNAGEL is PARKER LABORATORIES INC.
What is the Primary UDI-DI identifier for SIGNAGEL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ELECTRODE GEL.
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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