FDA Registration Active 🇮🇱 Israel

Baxter Healthcare - Tel Aviv

Reg #: 3005004021 · FEI: 3005004021 · Expires 2026
Products
7
Proprietary Names
30
Establishment Types
5
Classifications
7

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Registration Details

Registration Name
Baxter Healthcare - Tel Aviv
Registration Number
3005004021
FEI Number
3005004021
Status
Active
Expiry Year
2026
Initial Importer
No
Address
2A Hashlosha St. F-32
City
Tel Aviv
Country
IL

Regulatory Submissions

510(k) Number
K051904

Owner / Operator

Firm Name
BAXTER HEALTHCARE CORPORATION
Operator Number
1417572
Address
One Baxter Parkway
City
Deerfield
State
IL
Postal Code
60015
Country
US
Correspondent
Maha Nolasco

US Agent

Business Name
BAXTER HEALTHCARE CORPORATION
Contact Name
Maha Nolasco
Address
25212 W. IL Route 120, RLT-04
City
Round Lake
State
IL
ZIP
60073
Country
US
Phone
224 2706181

Products

Device Name Product Code
Blood Pressure Cuff DXQ
Plinth INT
Plethysmograph, Impedance DSB
System, Measurement, Blood-Pressure, Non-Invasive DXN
Oximeter DQA
Computer, Diagnostic, Pre-Programmed, Single-Function DXG
Oximeter, Ear DPZ

Proprietary Names

SunTech Cuff, All purpose general (Adult) SunTech Cuff, All purpose general (Adult Large) Passive Leg Raise Lift Reliant with SPo2 Cheetah Reliant Cheetah Nicom with NIBP Functionality Nicom Reliant with SPO2 Nicom Starling Monitor with SpO2 module Cheetah Nicom Nicom Reliant Cheetah Nicom Reliant Cheetah Starling SV Reliant Starling SV Starling Monitor Starling Fluid Management System Nicom – A Non-Invasive Cardiac Output Monitor Cheetah Nicom with NIBP and SpO2 Cheetah Nicom System NICOM Electrodes Prewired Electrode of Cheetah Medical Starling Sensors Electrode Cheetah Sensors Baxter Starling Sensor Pre-wired NICOM Sensor NICOM sensor OXIMAX PULSE OXIMETRY SYSTEM WITH N-595 PULSE OXIMETER AND OXIMAX SENSORS AND CABLES (AKA ACCESSORIES) Nelcore Adult SpO2 sensor and Pulse Oximetry Interface Cable

Establishment Types

Repack or Relabel Medical Device Export Device to the United States But Perform No Other Operation on Device Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility