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Holter Recorder – External Pacemaker – Stress Test – ECG ...
- http://www.galix-gbi.com/index.php
- As a designer and manufacturer of medical electronic equipment, Galix focuses primarily on the cardiology business. The company´s portfolio varies from Digital Holter Recorders …
Galix Biomedical Instrumentation Inc Company Profile
- https://www.dnb.com/business-directory/company-profiles.galix_biomedical_instrumentation_inc.05f5d604240b5bb2.html
- Address: 8205 NW 30TH Ter Doral, FL, 33122-1913 United States Website: www.galix-gbi.com
510(k) Premarket Notification - Food and Drug …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K092853
- 510 (k) Number. K092853. Device Name. 3 CHANNEL DIGITAL AMBULATORY ECG RECORDER MODEL GALIX GBI-3SM. Applicant. GALIX BIOMEDICAL …
Galix Biomedical Instrumentation - Headquarters …
- https://www.cbinsights.com/company/galix-biomedical-instrumentation
- Galix Biomedical Instrumentation is a medical device company. Use the CB Insights Platform to explore Galix Biomedical Instrumentation's full profile. Galix …
Transcutaneous Pacing Market 2023: Segment-Wise …
- https://www.marketwatch.com/press-release/transcutaneous-pacing-market-2023-segment-wise-market-analysis-and-growth-potential-2028-2023-02-14
- Oscor Galix Biomedical Instrumentation Osypka Medical CardioLogic StJude Medical . Get Sample Copy of Transcutaneous Pacing Market Report
Línea de Productos - Galix Biomedical …
- http://espanol.galix-gbi.com/product_line.php
- Línea de Productos - Galix Biomedical Instrumentation. Internacionalmente conocida como especialistas en grabadores Holter y marcapasos externos, la empresa se …
Galix Biomed Instrumentation - 2555 Collins Ave - BusinessYab
- https://www.businessyab.com/explore/united_states/florida/miami_dade_county/miami/mid_beach/collins_avenue/2555/galix-biomed-instrumentation-305-534-5905.html
- Galix Biomed Instrumentation is located in Miami-Dade County of Florida state. On the street of Collins Avenue and street number is 2555. To communicate or ask …
510(k) Premarket Notification
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K971670
- Date Received: 05/06/1997: Decision Date: 01/29/1998: Decision: Substantially Equivalent (SESE) Regulation Medical Specialty: Cardiovascular 510k Review Panel
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