gudid
Primary ID: 550128
COECIDE XL (UDI 550128)
Manufactured by Gc America Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COECIDE XL - Primary ID 550128
Device Regulatory Overview
The COECIDE XL (Model/Catalog Number: 550128) is a medical device manufactured by Gc America Inc.. This product is indexed under FDA Product Code / Category Classification MED within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 550128
- Product Code / EMDN
- MED
- Device Name
- COECIDE XL Plus 1 gallon liquid with 158g activator
- Database Sync Date
- 2026-08-09 09:03:07
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 COECIDE XL?
The registered manufacturer of record for COECIDE XL is Gc America Inc..
What is the Primary UDI-DI identifier for COECIDE XL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 550128.
What classification code is assigned to this device?
This device is registered under product classification code MED.
Similar Classification Devices (MED)
Other Devices by Gc America Inc.
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