gudid
Primary ID: MC20100-C0
MEDCUT (UDI MC20100-C0)
Manufactured by MEDAX SRL UNIPERSONALE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDCUT - Primary ID MC20100-C0
Device Regulatory Overview
The MEDCUT (Model/Catalog Number: MC20100-C0) is a medical device manufactured by MEDAX SRL UNIPERSONALE. This product is indexed under FDA Product Code / Category Classification KNW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MC20100-C0
- Product Code / EMDN
- KNW
- Device Name
- Automatic disposable biopsy system 20G X 100 M
- Database Sync Date
- 2026-08-09 09:04:29
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 MEDCUT?
The registered manufacturer of record for MEDCUT is MEDAX SRL UNIPERSONALE.
What is the Primary UDI-DI identifier for MEDCUT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MC20100-C0.
What classification code is assigned to this device?
This device is registered under product classification code KNW.
Similar Classification Devices (KNW)
Other Devices by MEDAX SRL UNIPERSONALE
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