gudid
Primary ID: C80G-021m
EXCOR (UDI C80G-021m)
Manufactured by Berlin Heart GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EXCOR - Primary ID C80G-021m
Device Regulatory Overview
The EXCOR (Model/Catalog Number: C80G-021m) is a medical device manufactured by Berlin Heart GmbH. This product is indexed under FDA Product Code / Category Classification DSQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C80G-021m
- Product Code / EMDN
- DSQ
- Device Name
- Arterial cannula for small children 6 mm; L 25 cm
- Database Sync Date
- 2026-08-09 09:17:36
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 EXCOR?
The registered manufacturer of record for EXCOR is Berlin Heart GmbH.
What is the Primary UDI-DI identifier for EXCOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C80G-021m.
What classification code is assigned to this device?
This device is registered under product classification code DSQ.
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