23 results · 45ms · Sources: EU EUDAMED, US FDA

TDXSP2-MCG TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx

FDA registration
INVACARE CORP. DBA INVACARE AMERICA·1 product·🇺🇸 United States

TDXSP2-MCG TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx

FDA registration
INVACARE CORP. DBA INVACARE AMERICA·1 product·🇺🇸 United States

Invacare® TDX® SP2 Power Wheelchair; TDXSP2 TDX SP2 with LiNX Electronics, TDXSP2-CG TDX SP2 Base for Single Act. System w/ Ultra Low Maxx, TDXSP2-MCG TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx

FDA 510(k)
FDA Class 2 ·Physical Medicine

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486003524·MCK FEMORAL TRIAL (SIZE 7 LM/RL)

n.a.

FDA UDI
Karl Storz GmbH & Co. KG·04048551058299·TRAUTMANN Mastoid Gouge, 14 cm

LEONE SPA

FDA UDI
LEONE SPA·08033707018698·CALIBRA 1ST MOLAR BANDS n.LL 7

XRES T

FDA registration
SORIN GROUP ITALIA S.R.L·1 product·🇮🇹 Italy

Zimmer Biomet Pty Ltd

FDA registration
Zimmer Biomet Pty Ltd·1 product·🇦🇺 Australia

ZIMMER PTE. LTD.

FDA registration
ZIMMER PTE. LTD.·1 product·🇸🇬 Singapore

MODIFICATION TO: LIGAFIX INTERFERENCE SCREW

FDA registration
Biomet Global Supply Chain Center B.V.·1 product·🇳🇱 Netherlands

ComposiTCP interference screws

FDA registration
SCIENCE & BIO MATERIALS, S.B.M. SAS·1 product·🇫🇷 France

Synergy Health Marseille SAS

FDA registration
Synergy Health Marseille SAS·1 product·🇫🇷 France

Zimmer (Shanghai) Medical International Trading Co., Ltd.

FDA registration
Zimmer (Shanghai) Medical International Trading Co., Ltd.·1 product·🇨🇳 China

XRES B

FDA registration
Steril Verona srl·1 product·🇮🇹 Italy

BioPlex 2200 ToRC IgM

FDA registration
Bio-Rad Laboratories, Inc.·6 products·🇺🇸 United States

FMI- Polyurethane PICC

FDA registration
FOOTPRINT MEDICAL INC.·1 product·🇺🇸 United States

SecurePortIV

FDA registration
H.B. Fuller Medical Adhesive Technologies, LLC·1 product·🇺🇸 United States

BioPlex 2200 ToRC IgM

FDA registration
BIO-RAD LABORATORIES, INC.·6 products·🇺🇸 United States

XRES BLOOD COLLECTION RESERVOIR

FDA 510(k)
FDA Class 2 ·Cardiovascular

MODIFICATION TO: LIGAFIX INTERFERENCE SCREW

FDA 510(k)
FDA Class 2 ·Orthopedic