Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3024821684

FEI Number

3024821684

Entity Name

RESPBUY HEALTHCARE

City/State/Country

Gurgaon Haryana, IN

Establishment Address

1ST FLOOR, A5-102, TULIP VIOLET, Gurgaon Haryana 122101, IN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Respbuy Healthcare (Owner Number: 10086374)

Owner / Operator Contact Address

Tulip Violet, Sec 69 Warehouse R2 130, M3M Corner Walk, Sec 74, Gurgaon, IN-HR 122002, IN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Airfit F20 Humidex

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BSJ	Mask, Gas, Anesthetic	Anesthesiology	Class 1	868.5550	2023-09-21
BTK	Strap, Head, Gas Mask	Anesthesiology	Class 1	868.5560	2022-11-03

Official Correspondent

Nelli Bielkova

US Agent Details

Nelli Bielkova Email: exitonb@yahoo.com Phone: (619) 5378340

Related Public Records

Same Entity

Respbuy Healthcare

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3024821684. Last updated year: 2026. Please use registration number 3024821684 when referencing this establishment in official correspondence.