10,000 results · 105ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Hudson RCI Oxygen Tubing Water Trap

FDA registration
Teleflex Medical Sdn. Bhd.·1 product·🇲🇾 Malaysia

AUTOJECT 2 (FIXED NEEDLE)

FDA registration
Owen Mumford Sdn Bhd·1 product·🇲🇾 Malaysia

GAMMEX PI PLUS GLOVE-IN-GLOVE SYSTEM TESTED FOR USE WITH CHEMOTHERAPY DRUGS

FDA registration
ANSELL SEREMBAN SDN. BHD·3 products·🇲🇾 Malaysia

NanoNeedle Scope 2

FDA registration
Altek Medical Sdn. Bhd.·1 product·🇲🇾 Malaysia

Patient Assistant

FDA registration
Plexus Manufacturing Sdn. Bhd.·1 product·🇲🇾 Malaysia

Patient Connector

FDA registration
Plexus Manufacturing Sdn. Bhd.·1 product·🇲🇾 Malaysia

DiamondTemp Generator Connection Box E

FDA registration
Plexus Manufacturing Sdn. Bhd.·1 product·🇲🇾 Malaysia

Rusch Standard FloCath

FDA registration
Teleflex Medical Sdn. Bhd.·1 product·🇲🇾 Malaysia

Rusch Endotracheal Tube Holder

FDA registration
Teleflex Medical Sdn. Bhd.·1 product·🇲🇾 Malaysia

VISCO TECHNOLOGY SDN. BHD

FDA registration
VISCO TECHNOLOGY SDN. BHD·1 product·🇲🇾 Malaysia

POWDER FREE NITRILE EXAMINATION GLOVE BLACK AND DURAL COLOR WHITE-BLUE

FDA registration
ANSELL SEREMBAN SDN. BHD·1 product·🇲🇾 Malaysia

KOON SENG SDN BHD

FDA registration
KOON SENG SDN BHD·1 product·🇲🇾 Malaysia

ANSELL N.P. SDN. BHD.

FDA registration
ANSELL N.P. SDN. BHD.·2 products·🇲🇾 Malaysia

ANSELL SEREMBAN SDN. BHD

FDA registration
ANSELL SEREMBAN SDN. BHD·1 product·🇲🇾 Malaysia

United Dragons Sdn. Bhd.

FDA registration
United Dragons Sdn. Bhd.·1 product·🇲🇾 Malaysia

ANSELL N.P. SDN. BHD.

FDA registration
ANSELL N.P. SDN. BHD.·1 product·🇲🇾 Malaysia

KOON SENG SDN BHD

FDA registration
KOON SENG SDN BHD·1 product·🇲🇾 Malaysia

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·UNIPOLAR/ LEAD END PIN CAP/OVAL PATCH LEAD

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·ACE HEADER/PATCH LEAD/LEAD END PIN CAP

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·End Cap, Epicardial Patch Lead, and Upsizing Sleeve