Stimulator, Low Electric Field, Tumor Treatment

FDA Pre-Market Approval

FDA Class 3 ·NOVOCURE LTD'S NOVOTTF-100A TREATMENT KIT

Stimulator, Low Electric Field, Tumor Treatment

FDA Pre-Market Approval

FDA Class 3 ·NOVOCURE LTD'S NOVOTTF-100A TREATMENT KIT

THERMO TEK IR FOREHEAD THERMOMETER, MODEL 718F

FDA 510(k)

FDA Class 2 ·General Hospital

MyNeoShield

FDA registration

MYLAB DISCOVERY SOLUTIONS PRIVATE LIMITED·1 product·🇮🇳 India

MyBox- Fluorescent Immunoassay Analyzer

FDA registration

MYLAB DISCOVERY SOLUTIONS PRIVATE LIMITED·1 product·🇮🇳 India

Viral Transport Medium with Lysis Soln. - Virotrap

FDA registration

MYLAB DISCOVERY SOLUTIONS PRIVATE LIMITED·1 product·🇮🇳 India

Compact MINI- Automated Nucleic Acid Extraction and qPCR Analysis System

FDA registration

MYLAB DISCOVERY SOLUTIONS PRIVATE LIMITED·1 product·🇮🇳 India

Automated Nucleic Acid Extraction and PCR Sample Preparation System- Compact X

FDA registration

MYLAB DISCOVERY SOLUTIONS PRIVATE LIMITED·1 product·🇮🇳 India

Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi

Manufacturer

🇹🇷 Türkiye·14122 Basic UDI-DIs·14863 Devices·HTCert (Health Technology Certification Ltd), HTCert (Health Technology Certification Ltd), HTCert (Health Technology Certification Ltd), HTCert (Health Technology Certification Ltd), UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş., UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş., UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş., UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş., UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş., UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş., and UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

Konix Anti-Fog Solution

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

GMR40

FDA 510(k)

FDA Class 2 ·Radiology

PATIENT EXAMINATION GLOVES (LATEX)

FDA 510(k)

FDA Class 1 ·General Hospital

INSTRUMENT TRAY 2, TK-5000 & TK-5001

Device

EU MDR · Eu Md Class 1 ·TeDan Surgical Innovations, Inc.·On the market·12 countries

INSTRUMENT TRAY 2, TK-5000 & TK-5001

Device

EU MDR · Eu Md Class 1 ·TeDan Surgical Innovations, Inc.·On the market·12 countries

INSTRUMENT TRAY 1, TK-5000 & TK-5001

Device

EU MDR · Eu Md Class 1 ·TeDan Surgical Innovations, Inc.·On the market·12 countries

Scaffold, Infrapopliteal, Absorbable

FDA Pre-Market Approval

FDA Class 3 ·Esprit™ BTK Everolimus Eluting Resorbable Scaffold System

Scaffold, Infrapopliteal, Absorbable

FDA Pre-Market Approval

FDA Class 3 ·Esprit™ BTK Everolimus Eluting Resorbable Scaffold System

Scaffold, Infrapopliteal, Absorbable

FDA Pre-Market Approval

FDA Class 3 ·Esprit™ BTK Everolimus Eluting Resorbable Scaffold System

Scaffold, Infrapopliteal, Absorbable

FDA Pre-Market Approval

FDA Class 3 ·Esprit™ BTK Everolimus Eluting Resorbable Scaffold System

Scaffold, Infrapopliteal, Absorbable

FDA Pre-Market Approval

FDA Class 3 ·Esprit™ BTK Everolimus Eluting Resorbable Scaffold System