SunMed Group Holdings, LLC dba AirLife

FDA registration

SunMed Group Holdings, LLC dba AirLife·1 product·🇺🇸 United States

QUIXIE NEBULIZER

FDA 510(k)

FDA Class 2 ·Anesthesiology

9340 2WAY BALOON VALVE

FDA UDI

HANS RUDOLPH, INC.·00874750009060·9340A 2WAY SHUT-OFF 22MM OD

REPAIR DEVICE

FDA registration

BIOMET, INC.·1 product·🇺🇸 United States

KLS Martin Resorb-X G (Oral Max)

FDA registration

BBF STERILISATIONSSERVICE GMBH·1 product·🇩🇪 Germany

KLS-Martin L.P.

FDA registration

KLS-Martin L.P.·1 product·🇺🇸 United States

Maxfire MarXmen

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

KLS Martin SE & Co. KG

FDA registration

KLS Martin SE & Co. KG·1 product·🇩🇪 Germany

Cuffs

FDA registration

TRACELOGIX CORPORATION·1 product·🇺🇸 United States

JMS SINGAPORE PTE. LTD

FDA registration

JMS SINGAPORE PTE. LTD·2 products·🇸🇬 Singapore

AIR PANTS

FDA registration

Allied Medical LLC·1 product·🇺🇸 United States

PT JMS BATAM

FDA registration

PT JMS BATAM·2 products·🇮🇩 Indonesia

MAXFIRE MARXMEN MENISCAL REPAIR DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

MODIFICATION TO: VECTORVISION FRAMELESS BIOPSY SYSTEM

FDA 510(k)

FDA Class 2 ·Neurology

Nebulizer (Direct Patient Interface)

FDA classification

FDA Class 2 ·Nebulizer (Direct Patient Interface)

Neurological Stereotaxic Instrument

FDA classification

FDA Class 2 ·Neurological Stereotaxic Instrument

Fastener, Fixation, Nondegradable, Soft Tissue

FDA classification

FDA Class 2 ·Fastener, Fixation, Nondegradable, Soft Tissue