gudid Primary ID: 2200-440Q

Meeker Hemostatic Forceps (UDI 2200-440Q)

Manufactured by SONTEC INSTRUMENTS, INC.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Meeker Hemostatic Forceps (Model/Catalog Number: 2200-440Q) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification HRQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2200-440Q
Product Code / EMDN: HRQ
Device Name: Meeker Hemostatic Forceps Right Angle Quantum
Database Sync Date: 2026-08-09 09:07:00

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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Frequently Asked Questions

Who is the primary manufacturer of Meeker Hemostatic Forceps?

The registered manufacturer of record for Meeker Hemostatic Forceps is SONTEC INSTRUMENTS, INC..

What is the Primary UDI-DI identifier for Meeker Hemostatic Forceps?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2200-440Q.

What classification code is assigned to this device?

This device is registered under product classification code HRQ.

Similar Classification Devices (HRQ)

Other Devices by SONTEC INSTRUMENTS, INC.

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