gudid
Primary ID: E10-BOXED
ELECTRO-GEL 32 OZ. BOXED (UDI E10-BOXED)
Manufactured by ELECTRO-CAP INTERNATIONAL INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELECTRO-GEL 32 OZ. BOXED - Primary ID E10-BOXED
Device Regulatory Overview
The ELECTRO-GEL 32 OZ. BOXED (Model/Catalog Number: E10-BOXED) is a medical device manufactured by ELECTRO-CAP INTERNATIONAL INC. This product is indexed under FDA Product Code / Category Classification GYB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E10-BOXED
- Product Code / EMDN
- GYB
- Device Name
- Database Sync Date
- 2026-08-09 09:22:15
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 ELECTRO-GEL 32 OZ. BOXED?
The registered manufacturer of record for ELECTRO-GEL 32 OZ. BOXED is ELECTRO-CAP INTERNATIONAL INC.
What is the Primary UDI-DI identifier for ELECTRO-GEL 32 OZ. BOXED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E10-BOXED.
What classification code is assigned to this device?
This device is registered under product classification code GYB.
Similar Classification Devices (GYB)
Other Devices by ELECTRO-CAP INTERNATIONAL INC
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