23 results
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45ms
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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