PE-210A

FDA registration

Nihon Kohden Corporation - Eastern Japan Logistics Center·2 products·🇯🇵 Japan

PE-210A

FDA registration

NIHON KOHDEN CORP.·2 products·🇯🇵 Japan

PE-210A

FDA registration

NIHON KOHDEN TOMIOKA PRODUCTION CENTER·2 products·🇯🇵 Japan

PE-210A

FDA registration

NIHON KOHDEN AMERICA, INC.·2 products·🇺🇸 United States

PE-210A

FDA registration

Nihon Kohden Corporation - Tokorozawa establishment Advanced Technology Center·2 products·🇯🇵 Japan

PE-210A

FDA registration

Nihon Kohden Tomioka Corporation·2 products·🇯🇵 Japan

PE-210AK SWITCH BOX

FDA 510(k)

FDA Class 2 ·Neurology

Medtronic Reusable Instruments

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00721902096211·ADJUSTER 9110376 IMPLANT TPRD 16MM

Full-Montage Standard Electroencephalograph

FDA classification

FDA Class 2 ·Full-Montage Standard Electroencephalograph

Utrecht Interstitial Fletcher CT/MR Applicator

FDA UDI

Nucletron B.V.·08717213035010·Interstitial Ovoid Pair 40mm, 15 °, R12.5

Synergy Health Daniken AG

FDA registration

Synergy Health Daniken AG·2 products·🇨🇭 Switzerland

Reprocessed Ultrasound Catheter

FDA registration

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

Ultrasound Catheter

FDA registration

Nypro Inc (Maple Grove)·1 product·🇺🇸 United States

AxSOS

FDA registration

STRYKER GmbH·2 products·🇨🇭 Switzerland

Isomedix Operations, Inc.

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

STERIGENICS UK LIMITED

FDA registration

STERIGENICS UK LIMITED·1 product·🇬🇧 United Kingdom

Solta Medical, Inc.

FDA registration

Solta Medical, Inc.·1 product·🇺🇸 United States

REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

EVERON CENTRAL DISPLAY STATION - CDS, MODEL VERSION 1.0.0

FDA 510(k)

FDA Class 2 ·Cardiovascular

Reprocessed Intravascular Ultrasound Catheter

FDA classification

FDA Class 2 ·Reprocessed Intravascular Ultrasound Catheter