15 results
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36ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Mermaid Medical® Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007000·Mermaid Medical® Guidewire .035” x 90 cm, 7.5 c...
Mermaid Medical® Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007062·Mermaid Medical® Guidewire .035” x 180 cm, 3.5 ...
Mermaid Medical® Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007079·Mermaid Medical® Guidewire .035” x 260 cm, 7.5 ...
ReShape Medical™ Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007109·ReShape Medical™ Guidewire .035” x 260 cm, 13 c...
Mermaid Medical® Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007055·Mermaid Medical® Guidewire .035” x 180 cm, 7.5 ...
Mermaid Medical® Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007031·Mermaid Medical® Guidewire .035” x 150 cm, 7.5 ...
Mermaid Medical® Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007017·Mermaid Medical® Guidewire .035” x 90 cm, 3.5 c...
Mermaid Medical® Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007048·Mermaid Medical® Guidewire .035” x 150 cm, 3.5 ...
Mermaid Medical® Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007024·Mermaid Medical® Guidewire .035” x 90 cm, 7.5 c...
Mermaid Medical® Guidewire
FDA UDI
TECHDEVICE CORPORATION·00850758007086·Mermaid Medical® Guidewire .035” x 260 cm, 3.5 ...
RIGIFLEX SINGLE-USE ACHALASIA BALLOON DILATOR
FDA Adverse Event
Malfunction
·TECHDEVICE CORPORATION·Product code KNQ·February 18, 2010
RIGIFLEX SINGLE-USE ACHALASIA BALLOON DILATOR
FDA Adverse Event
Malfunction
·TECHDEVICE CORPORATION·Product code KNQ·February 18, 2010
RIGIFLEX SINGLE-USE ACHALASIA BALLOON DILATOR
FDA Adverse Event
Malfunction
·TECHDEVICE CORPORATION·Product code KNQ·November 8, 2010
RIGIFLEX II ACHALASIA BALLOON DILATOR
FDA Adverse Event
Malfunction
·TECHDEVICE CORPORATION·Product code KNQ·October 4, 2011
RADIFOCUS GLIDEWIRE ADVANTAGE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 23, 2022