gudid
Primary ID: UN18300-00
UNIVERSAL (UDI UN18300-00)
Manufactured by MEDAX SRL UNIPERSONALE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UNIVERSAL - Primary ID UN18300-00
Device Regulatory Overview
The UNIVERSAL (Model/Catalog Number: UN18300-00) 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
- UN18300-00
- Product Code / EMDN
- KNW
- Device Name
- Biopsy needle 18G x 300 mm
- 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 UNIVERSAL?
The registered manufacturer of record for UNIVERSAL is MEDAX SRL UNIPERSONALE.
What is the Primary UDI-DI identifier for UNIVERSAL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UN18300-00.
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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