NETEERA TECHNOLOGIES LTD

FDA Device Registration & Listing · Jerusalem, IL · Registration 3014739036

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014739036
FEI Number
3014739036
Entity Name
NETEERA TECHNOLOGIES LTD
City/State/Country
Jerusalem, IL
Establishment Address
Prof. Rakah 3 st., Jerusalem 9270403, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Neteera Technologies LTD (Owner Number: 10077846)
Owner / Operator Contact Address
Prof. Rakah St 3, Jerusalem, IL-JM 9270403, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Neteera 130H/131H Vital Sign Monitoring Sensor

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) Cardiovascular Class 2 870.2300 2022-10-20
BZQ Monitor, Breathing Frequency Anesthesiology Class 2 868.2375 2022-10-20

Official Correspondent

Shimon Steinberger

US Agent Details

Yasser E Sadek Business: Hudson Scientific LLC Email: Yasser@hudsci.com Phone: (206) 6069598

Related Public Records

Same Entity

Neteera Technologies 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
K832250 Litton Medical Electronics SERVOMED BASIC BEDSIDE UNIT SMA 102- 1984-06-01
K801515 Abbott Medical Electronics Co. ABBY II PATIENT MONITOR OR VITAL SIGNS M 1980-07-08
K913749 Edentec Corp. EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170 1992-07-02
K771407 Research Development Corp. LUNG VOLUME & PRESSURE MONITOR 1977-08-04
K122223 Philips Medizin Systeme Boeblingen GmbH NEW: INTELLIVUE CL RESPIRATION POD NEW: SPECIALIZED ASSESSORY: MOBILE CL RESP ATTACHMENT MODIFIED: INTELLIVUE PATIENT MO 2013-04-12

Similar Registrations

Registration Number Establishment Name Location
1062836 DIGICARE BIOMEDICAL TECHNOLOGY, INC. BOYNTON BEACH, FL, US
3009499478 EDAN Diagnostics, Inc. San Diego, CA, US
3009156722 SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. Shenzhen Guangdong, CN
3017760831 Hi-P ELECTRONICS (MALAYSIA) SDN. BHD. Kulim Kedah, MY
3007305624 GUANGDONG BIOLIGHT MEDITECH CO., LTD Zhuhai Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014739036. Last updated year: 2026. Please use registration number 3014739036 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.