GUDIDData
gudid Primary ID: N02A08201F

Suction Catheter (UDI N02A08201F)

Manufactured by Well Lead Medical Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Suction Catheter - Primary ID N02A08201F

Device Regulatory Overview

The Suction Catheter (Model/Catalog Number: N02A08201F) is a medical device manufactured by Well Lead Medical Co.,Ltd. This product is indexed under FDA Product Code / Category Classification BSY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
N02A08201F
Product Code / EMDN
BSY
Device Name
Curved tip Suction Catheter Cap-cone connector 20Fr
Database Sync Date
2026-08-09 09:04:58

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Suction Catheter?

The registered manufacturer of record for Suction Catheter is Well Lead Medical Co.,Ltd.

What is the Primary UDI-DI identifier for Suction Catheter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is N02A08201F.

What classification code is assigned to this device?

This device is registered under product classification code BSY.

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