79 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Vantage® Total Ankle System
FDA 510(k)
FDA Class 2
·Orthopedic
Introcan Safety ® 2
FDA UDI
B. BRAUN MEDICAL INC.·04046955341818·Introcan Safety 2 - 24G x 0.75 in., PUR, Straight
Channel
FDA UDI
MEDTRONIC PS MEDICAL, INC.·00643169103573·NEUROENDOSCOPE 2232-002 CHANNEL 3.5
ChannelScope, Long, 10K
FDA UDI
CLARUS MEDICAL, LLC·00810004820937·ChannelScope, 10K Pixels, Long, 21.6cm Working ...
N/A
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024369368·THOMAS LEG SPLINT RADIOLUCENT SMALL
FERTELL FEMALE FERTILITY TEST
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SINGLE USE SOFT TIPPED DISPOSABLE INJECTOR, RAYSERT SINGLE USE SOFT TIPPED SMALL INCISION DISPOSABLE INJECTOR
FDA 510(k)
FDA Class 1
·Ophthalmic
HAMILTON MEDICAL AG
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·July 12, 2023
HAMILTON MEDICAL AG
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·July 10, 2023
HAMILTON-C1
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·July 31, 2024
HAMILTON-C1
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·May 10, 2024
Cable-Ready®
FDA UDI
Zimmer, Inc.·00889024039377·
Cable-Ready®
FDA UDI
Zimmer, Inc.·00889024039438·
Cable-Ready®
FDA UDI
Zimmer, Inc.·00889024039360·
PULMONETIC
FDA Adverse Event
Malfunction
·PULMONETIC SYSTEMS, INC.·Product code CBK·January 22, 2003
KMI WRIST FUSION SYSTEM
FDA Adverse Event
Injury
·KINETIKOS MEDICAL, INC.·Product code HRS·July 23, 2002
HAMILTON-C1
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·August 23, 2024
HAMILTON MEDICAL AG
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·April 17, 2023
HAMILTON-C1
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·October 2, 2024
HAMILTON MEDICAL AG
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·July 13, 2023