gudid Primary ID: MOSQUITO FORCEPS

FORCEPS (UDI MOSQUITO FORCEPS)

Manufactured by DR.FRIGZ INTERNATIONAL(PVT)LTD,

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FORCEPS (Model/Catalog Number: MOSQUITO FORCEPS) is a medical device manufactured by DR.FRIGZ INTERNATIONAL(PVT)LTD,. This product is indexed under FDA Product Code / Category Classification HRQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MOSQUITO FORCEPS
Product Code / EMDN: HRQ
Device Name: MOSQUITO FCP 3-1/2"
Database Sync Date: 2026-08-09 09:06:20

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 FORCEPS?

The registered manufacturer of record for FORCEPS is DR.FRIGZ INTERNATIONAL(PVT)LTD,.

What is the Primary UDI-DI identifier for FORCEPS?

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

What classification code is assigned to this device?

This device is registered under product classification code HRQ.

Similar Classification Devices (HRQ)

Other Devices by DR.FRIGZ INTERNATIONAL(PVT)LTD,

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