25 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Albumin BCP2
FDA 510(k)
FDA Class 2
·Clinical Chemistry
n.a.
FDA UDI
Karl Storz GmbH & Co. KG·04048551067031·Suction Tube, conical, dia. 3 mm
16PW - Burn Relief
FDA UDI
Certified Safety Manufacturing, Inc.·00766588030302·16PW - Burn Relief
Needle aspiration and injection
FDA UDI
KATENA PRODUCTS, INC.·00841668113639·RETROBULBAR NEEDLE 25GA 38MM
Safety T-Pin
FDA UDI
TP ORTHODONTICS INC·00192029028360·Stainless Steel Oriented
NorthStar
FDA UDI
Seaspine Orthopedics Corporation·10889981197445·Smooth Shank Poly. Screw, 3.5mm x 30mm
HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED)
FDA 510(k)
FDA Class 2
·Ophthalmic
SPIRODOC
FDA 510(k)
FDA Class 2
·Anesthesiology
Gibralt®
FDA UDI
INNO Holdings, Inc.·M711050002035300·Posterior Cervical Screw Assembly, 3.5mm X 30mm...
Gibralt
FDA UDI
Choice Spine, LP·10885862247537·
CVC KIT: 2-LUMEN 7 FR X 16 CM
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code DQO·October 17, 2008
CAPSURE SP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·July 3, 2013
36MM COCR BIOMET FEM HD -3 NK
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HRY·September 6, 2018
VASSALLO GT
FDA Adverse Event
Injury
·FILMECC CO., LTD.·Product code DQX·October 3, 2024
RINGLOC 36MM EPOLY LNR 10 DEG SZ24
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·August 31, 2018
2.0 MM SS CABLE/SLEEVE COMBO
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDQ·August 31, 2018
2.0 MM SS CABLE/SLEEVE COMBO
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDQ·August 31, 2018
REGEN/RNGLC+ MULTI 56MM SZ 24
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 31, 2018
ARCOS CON SZ B STD 60MM HA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·August 31, 2018