eudamed_udi
Primary ID: 08429659014503
coverpack (UDI 08429659014503)
Manufactured by CARDIVAIS S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for coverpack - Primary ID 08429659014503
Device Regulatory Overview
The coverpack (Model/Catalog Number: 2LC020013) is a medical device manufactured by CARDIVAIS S.A.. This product is indexed under FDA Product Code / Category Classification A03020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2LC020013
- Product Code / EMDN
- A03020102
- Device Name
- HP Lines
- Database Sync Date
- 2026-08-09 16:28:44
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 coverpack?
The registered manufacturer of record for coverpack is CARDIVAIS S.A..
What is the Primary UDI-DI identifier for coverpack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08429659014503.
What classification code is assigned to this device?
This device is registered under product classification code A03020102.
Similar Classification Devices (A03020102)
Other Devices by CARDIVAIS S.A.
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