eudamed_udi
Primary ID: 00659443000049
Precision Flow Tubing (UDI 00659443000049)
Manufactured by KORU Medical Systems, Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Precision Flow Tubing - Primary ID 00659443000049
Device Regulatory Overview
The Precision Flow Tubing (Model/Catalog Number: F2) is a medical device manufactured by KORU Medical Systems, Inc. This product is indexed under FDA Product Code / Category Classification A0399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F2
- Product Code / EMDN
- A0399
- Device Name
- Precision Flow Tubing
- Database Sync Date
- 2026-08-09 16:29:31
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 Precision Flow Tubing?
The registered manufacturer of record for Precision Flow Tubing is KORU Medical Systems, Inc.
What is the Primary UDI-DI identifier for Precision Flow Tubing?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00659443000049.
What classification code is assigned to this device?
This device is registered under product classification code A0399.
Similar Classification Devices (A0399)
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