3,691 results · 35ms · Sources: EU EUDAMED, US FDA

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DEOMED BAMBOO LONG

Device
EU MDR · Eu Md Class 1 ·JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin·On the market

DEOMED COTTON SILVER

Device
EU MDR · Eu Md Class 1 ·JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin·On the market

DEOMED BAMBOO LONG

Device
EU MDR · Eu Md Class 1 ·JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin·On the market

DEOMED BAMBOO LONG

Device
EU MDR · Eu Md Class 1 ·JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin·On the market

DEOMED BAMBOO LONG

Device
EU MDR · Eu Md Class 1 ·JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin·On the market

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval
FDA Class 3 ·Master Restore, Itrel®, Synergy®, Intellis™ and Vanta™ Spinal Cord Stimulation Systems and Pisces™, Specify®, Vectris® S

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·CROSS SAIL CORONARY DILATATION CATHETER

Auto Tono/Refracto/Kerato/Pachymeter HTR-1A

FDA UDI
Huvitz Co., Ltd.·08800019600558·Auto Tono/Refracto/Kerato/Pachymeter HTR-1A

Visionix VX650

FDA UDI
LUNEAU TECHNOLOGY OPERATIONS·03664188000145·

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CONTAK RENEWAL, CONTAK RENEWAL 3, CONTAK RENEWAL 3 HE, CONTAK RENEWAL E RF, CONTAK RENEWAL 3 RF HE W/CONSULT PROG SFTWR

ADULT-SINGLE-HHW-WITH CB

Device
EU MDD · Eu Md Class 2a ·Foxxmed Ltd·On the market·1 country

Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia

FDA Pre-Market Approval
FDA Class 3 ·MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear

Approach

FDA UDI
COOK INCORPORATED·00827002529380·Approach, Hydro ST Micro Wire Guide with Hydrop...

Approach

FDA UDI
COOK INCORPORATED·00827002529373·Approach, Hydro ST Micro Wire Guide with Hydrop...

Approach

FDA UDI
COOK INCORPORATED·00827002529397·Approach, Hydro ST Micro Wire Guide with Hydrop...

Implant, Intragastric For Morbid Obesity

FDA Pre-Market Approval
FDA Class 3 ·LAP-BAND ADJUSTABLE GASTRIC BANDING (LAGB) SYSTEM

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MODEL 2490G/H/J MEDTRONIC CARELINK MONITOR AND THE MODEL 2020A CARDIOSIGHT READER

HOW Plier Curved

Basic UDI-DI
EU MDR · Eu Md Class 1 ·Medspo·1 device

HOW Plier Straight

Basic UDI-DI
EU MDR · Eu Md Class 1 ·Medspo·1 device

HOW PLIER STR

Basic UDI-DI
EU MDR · Eu Md Class 1 ·Dental Expert·1 device