21 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ViperCath XC Peripheral Exchange Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
X-CORE
FDA UDI
Nuvasive, Inc.·00887517293985·X-CORE 2 Ti Endcap, Ø18x18x30mm 0°
22MM SMOOTHBORE EXHALATION VALVE BREATHING SYSTEM WITH MONITORING LINE 1.6M
FDA UDI
Intersurgical Incorporated·05030267069750·22MM SMOOTHBORE EXHALATION VALVE BREATHING SYST...
X-CORE
FDA UDI
Nuvasive, Inc.·00887517244369·X-CORE 2 Ti Endcap, Ø16x18x30mm 0°
V. Mueller
FDA UDI
STERIS CORPORATION·10885403279249·V. Mueller DISPOSABLE BIPOLAR FORCEPS
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304270350·
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100936·JAFFE LID RETRACTOR LARGE
SMART READ BIOLOGICAL TEST PACK
FDA 510(k)
FDA Class 2
·General Hospital
INTEGRA TOTAL FOOT SYSTEMS
FDA 510(k)
FDA Class 2
·Orthopedic
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197456593·Harken Rib and Scapula Spreader, compl.
210x65...
NA
FDA UDI
STRYKER CORPORATION·04546540042262·2108 Series Sagittal Blade, No Offset (28.9 x ...
IMPELLA 5.5
FDA Adverse Event
Malfunction
·ABIOMED, INC.·Product code OZD·October 18, 2023
Ascend
FDA UDI
ALPHATEC SPINE, INC.·00190376521039·12 mm CORE ENDPLATE, BAN 18 x 30 mm 0°
Ascend
FDA UDI
ALPHATEC SPINE, INC.·00190376521398·16 mm CORE ENDPLATE, BAN 18 x 30 mm 0°
642E Centrifuge, Billings
FDA UDI
DRUCKER DIAGNOSTICS·00810052861296·General purpose laboratory centrifuge for sampl...
CONTOUR PLUS
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·December 3, 2024
AMPLATZER AMULET
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NGV·March 19, 2024
RX ACCUNET EMBOLIC PROTECTION SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NTE·June 21, 2013
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·July 28, 2011
LOW PRESSURE BLACK MAX HANDPIECE
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBB·October 17, 2014