gudid
Primary ID: BF16100-02
BIO-FEATHER (UDI BF16100-02)
Manufactured by MEDAX SRL UNIPERSONALE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BIO-FEATHER - Primary ID BF16100-02
Device Regulatory Overview
The BIO-FEATHER (Model/Catalog Number: BF16100-02) 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
- BF16100-02
- Product Code / EMDN
- KNW
- Device Name
- Semi-automatic disposable biopsy system with adjustable penetration depth 16G X 100 MM
- Database Sync Date
- 2026-08-09 09:04:28
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BIO-FEATHER?
The registered manufacturer of record for BIO-FEATHER is MEDAX SRL UNIPERSONALE.
What is the Primary UDI-DI identifier for BIO-FEATHER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BF16100-02.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint