25 results · 32ms · Sources: EU EUDAMED, 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