gudid
Primary ID: 500 mL
Alcavis 50 (UDI 500 mL)
Manufactured by Angelini Pharma Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alcavis 50 - Primary ID 500 mL
Device Regulatory Overview
The Alcavis 50 (Model/Catalog Number: 500 mL) is a medical device manufactured by Angelini Pharma Inc.. This product is indexed under FDA Product Code / Category Classification KDJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 500 mL
- Product Code / EMDN
- KDJ
- Device Name
- Electrolytic Chloroxidizer High Level Disinfectant.
- Database Sync Date
- 2026-08-09 09:46:57
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 Alcavis 50?
The registered manufacturer of record for Alcavis 50 is Angelini Pharma Inc..
What is the Primary UDI-DI identifier for Alcavis 50?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 500 mL.
What classification code is assigned to this device?
This device is registered under product classification code KDJ.
Similar Classification Devices (KDJ)
Other Devices by Angelini Pharma Inc.
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