Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013429468

FEI Number

3013429468

Entity Name

QUALITY IN FLOW LTD.

City/State/Country

PETAH TIKVA Central, IL

Establishment Address

23 HA-YETSIRA st., PETAH TIKVA Central 4951251, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Quality in Flow Ltd. (Owner Number: 10053030)

Owner / Operator Contact Address

23 HA-YETSIRA st., PETAH TIKVA, IL-M 4951251, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K211800

PMA Number

N/A

All Registered Proprietary Names

Warrior Warrior Blood and Fluid Warmer QiF device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BSB	Warmer, Blood, Non-Electromagnetic Radiation	Hematology	Class 2	864.9205	2017-12-24
LGZ	Warmer, Thermal, Infusion Fluid	General Hospital	Class 2	880.5725	2017-12-24
BSB	Warmer, Blood, Non-Electromagnetic Radiation	Hematology	Class 2	864.9205	2018-12-11
LGZ	Warmer, Thermal, Infusion Fluid	General Hospital	Class 2	880.5725	2018-12-11
LGZ	Warmer, Thermal, Infusion Fluid	General Hospital	Class 2	880.5725	2019-07-25
BSB	Warmer, Blood, Non-Electromagnetic Radiation	Hematology	Class 2	864.9205	2019-07-25
BSB	Warmer, Blood, Non-Electromagnetic Radiation	Hematology	Class 2	864.9205	2022-12-19
LGZ	Warmer, Thermal, Infusion Fluid	General Hospital	Class 2	880.5725	2022-12-19

Official Correspondent

Omer Pechter

US Agent Details

Ariel Katz Email: ariel.katz@qinflow.com Phone: (469) 6825356

Related Public Records

Same Entity

Quality in Flow Ltd.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K090508	Belmont Instrument Corp.	THE BELMONT BUDDY LITE FLUID WARMER	2009-03-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013429468. Last updated year: 2026. Please use registration number 3013429468 when referencing this establishment in official correspondence.