28 results · 30ms · Sources: EU EUDAMED, US FDA

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Tasso+ Convenience Kit

FDA UDI
Tasso Inc.·00860006434571·Tasso+ convenience kit allows self-collection o...

AFFIRM DO DIODE LASER

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Dynamic Axial Fixator

FDA UDI
ORTHOFIX SRL·18032568032109·CANNULATED DRILL BIT D 4.8 MM LENGTH 250 MM

TeleRehab Software File Manager

FDA UDI
SCOTTCARE CORPORATION, THE·00856298006244·The ScottCare VersaCare Cardiopulmonary Monitor...

Tasso+ Convenience Kit

FDA UDI
Tasso Inc.·00860006434526·Tasso+ allows self-collection of a capillary bl...

Innomed, Inc.

FDA UDI
INNOMED, INC.·00840277126092·Kolbel Self-Retaining Retr w/Hinge, Dbl Ergo Hd...

GUTTA PERCHA POINTS

FDA UDI
DiaDent Group International·08806383501743·Gutta Percha Points is used to root canal filin...

OrthoMedFlex

FDA UDI
ORTHOMEDFLEX LLC·M7161016010·Kratos Tray, Bonded Stem

L1

FDA UDI
KLS-Martin L.P.·00888118142016·BASE, UNIVERSAL, PLATE LEVEL

Innomed, Inc.

FDA UDI
INNOMED, INC.·00840277124913·Kolbel Self-Retaining Retr w/Hinge, Dbl Ergo Ha...

ARDO SUCTION PUMP MASTER, MODEL 30.00.XX; ARDO SUCTION PUMP SENATOR, MODEL 31.00.XX

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DISPOSABLE PVC POWDERED SYNTHETIC EXAM GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

PAINSMART IOD

FDA Adverse Event
Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 30, 2013

HYGIENIKIT

FDA Adverse Event
Injury ·AMEDA INC.·Product code HGY·August 27, 2014

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 11, 2011

ARTICULEZE M HEAD 36MM +5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·May 8, 2013

PINNACLE MTL INS NEUT36IDX54OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 8, 2013

UNK - CAGE/SPACERS: SYNCAGE

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code MAX·November 10, 2020

PINNACLE MTL INS NEUT36IDX54OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·September 19, 2012

UNKNOWN DEPUY DEVICE

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·September 19, 2012