GUDIDData
gudid Primary ID: 10-096-02

ENT Suction Tube #2 (UDI 10-096-02)

Manufactured by N S SURGICAL COMPANY

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ENT Suction Tube #2 - Primary ID 10-096-02

Device Regulatory Overview

The ENT Suction Tube #2 (Model/Catalog Number: 10-096-02) is a medical device manufactured by N S SURGICAL COMPANY. This product is indexed under FDA Product Code / Category Classification JZF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10-096-02
Product Code / EMDN
JZF
Device Name
A hand-held surgical instrument, formed in the shape of a tube, used to provide dissection while controlling intraoperative bleeding, and for the removal of debris/fluids, during ear/nose/throat (ENT) surgery. The device is connected to the tubing of a suction system at the proximal end and there is an opening at the working end through which the suction is applied to the site. The distal end is typically shaped as a rounded, flat blade, allowing the two functions to be applied simultaneously. It will have fingertip suction control and eliminates the need for a separate suction tip. It is made of metal and comes in various shapes and sizes. This is a reusable device.
Database Sync Date
2026-08-09 09:03:58

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 ENT Suction Tube #2?

The registered manufacturer of record for ENT Suction Tube #2 is N S SURGICAL COMPANY.

What is the Primary UDI-DI identifier for ENT Suction Tube #2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-096-02.

What classification code is assigned to this device?

This device is registered under product classification code JZF.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint