4,346 results · 43ms · Sources: EU EUDAMED, US FDA

Air/Water Syringe Tips

Basic UDI-DI
EU MDR · Eu Md Class 2a ·Suzhou Pac-Dent Technology Co., Ltd.·9 devices

Surgical Aspirator Tips

Basic UDI-DI
EU MDR · Eu Md Class 2a ·Suzhou Pac-Dent Technology Co., Ltd.·3 devices

Dental root-canal Instruments

Basic UDI-DI
EU MDR · Eu Md Class 2a ·Suzhou Pac-Dent Technology Co., Ltd.·146 devices

CR-03-1087-817-23

Certificate
MDR QMS·Nexstim Plc·Eurofins Electric & Electronics Finland Oy

EUFI29-21000160-S

Certificate
MDD Annex II (excluding section 4)·Nexstim Plc·Eurofins Electric & Electronics Finland Oy·3 Basic UDI-DIs

Disposable Laryngoscope Blade

Basic UDI-DI
EU MDD · Eu Md Class 1 ·Hangzhou Tappa Medical Technology Co , Ltd.·1 device

Clear Guide CORE

FDA UDI
CLEAR GUIDE MEDICAL, INC.·B201CGCORE24MR0·The device is intended as a computer platform t...

Clear Guide CORE

FDA UDI
CLEAR GUIDE MEDICAL, INC.·B201CGCORE130·The device is intended as a computer platform t...

Clear Guide CORE

FDA UDI
CLEAR GUIDE MEDICAL, INC.·B201CGCORE240·The device is intended as a computer platform t...

SARNS 8000 MODULAR PERFUSION SYSTEM

FDA registration
TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·7 products·🇺🇸 United States

LANAMER P.C.

Importer
1 Manufacturer

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing

FDA Pre-Market Approval
FDA Class 3 ·LCS TOTAL KNEE SYSTEM

TigerView

FDA UDI
TELEVERE SYSTEMS, LLC·00851800007108·TigerView software version 8.4.1

TigerView

FDA UDI
TELEVERE SYSTEMS, LLC·00851800007085·TigerView software version 8.2

ExamVue PACS

FDA UDI
TELEVERE SYSTEMS, LLC·00851800007078·ExamVue PACS version 1.1 Build 81

TigerView

FDA UDI
TELEVERE SYSTEMS, LLC·00851800007061·TigerView software version 8.3

TigerView

FDA UDI
TELEVERE SYSTEMS, LLC·00851800007009·TigerView Pro software version 7.7.13

TigerView

FDA UDI
TELEVERE SYSTEMS, LLC·00851800007023·TigerView Pro software version 7.7.3

TigerView

FDA UDI
TELEVERE SYSTEMS, LLC·00851800007016·TigerView 8.1 software Build 81

LumiGuide Wire; LumiGuide Equipment R2.0; LumiGuide 3D Hub

FDA 510(k)
FDA Class 2 ·Cardiovascular