10,000 results
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51ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TUFFease®
FDA UDI
Innovative Medical Products, Inc·00696588002996·TUFFease® Leg Extension Gel Pad 36" x 12" x 1/2"
AvalancheLase
FDA UDI
FOTONA d.o.o.·03830054230361·The AvalancheLase Family is based on Nd:YAG (10...
POWER CHAIR 20 WIDE BY 18 DEEP FOR PMI
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·January 7, 2015
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·December 14, 2011
SCLERAL BUCKLING DEVICE
FDA Adverse Event
Injury
·UNK·Product code LXP·April 19, 2000
Plug, Scleral
FDA classification
FDA Class 2
·Plug, Scleral
SPFM, L.P.
FDA registration
SPFM, L.P.·1 product·🇺🇸 United States
SLZ 5XP TBL
FDA UDI
KEELER LIMITED·05055272715331·
SLZ 3XP REF
FDA UDI
KEELER LIMITED·05055272715232·
SLZ 3XP TBL
FDA UDI
KEELER LIMITED·05055272715249·
SLZ 5XP REF
FDA UDI
KEELER LIMITED·05055272715324·
KLS-Martin L.P.
FDA registration
KLS-Martin L.P.·157 products·🇺🇸 United States
ENCORE MEDICAL, L.P.
FDA registration
ENCORE MEDICAL, L.P.·69 products·🇺🇸 United States
GALDERMA LABORATORIES, L.P.
FDA registration
GALDERMA LABORATORIES, L.P.·4 products·🇺🇸 United States
SLZ 3XP DiR REF
FDA UDI
KEELER LIMITED·05055272715294·
SLZ 3XP Di TBL
FDA UDI
KEELER LIMITED·05055272715270·
SLZ 3XP Di REF
FDA UDI
KEELER LIMITED·05055272715263·
SLZ 3XP TBL USA
FDA UDI
KEELER LIMITED·05055272715256·
SLZ 5XP Di TBL
FDA UDI
KEELER LIMITED·05055272715362·
SLZ 5XP DI REF
FDA UDI
KEELER LIMITED·05055272715355·