Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011802696

FEI Number

3011802696

Entity Name

QNQ Design and Development Pvt. Ltd.

City/State/Country

New Delhi, IN

Establishment Address

253, Okhla Industrial Estate, Phase-3, New Delhi 110020, IN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

CM Technologies, Inc. (Owner Number: 10049590)

Owner / Operator Contact Address

1321 Valwood Parkway,, Suite 530,, Carrollton, TX 75006, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

QiVi Lite Male External Urine Management Device Qoramatic, Qoramatic Drainage Bags

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NOA	Device, Paste-On For Incontinence, Non-Sterile	Gastroenterology, Urology	Class 1	876.5250	2021-10-06
KDQ	Bottle, Collection, Vacuum	General Hospital	Class 2	880.6740	2021-10-06

Official Correspondent

No official correspondent registered.

US Agent Details

Alan Donald Business: Matrix Medical Consulting, Inc. Email: adonald@me.com Phone: (619) 2085624

Related Public Records

Same Entity

CM Technologies, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3013524793	CM Technologies, Inc.	Carrollton, TX, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011802696. Last updated year: 2026. Please use registration number 3011802696 when referencing this establishment in official correspondence.