2,137 results · 36ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Puriblood

FDA UDI
PURIBLOOD MEDICAL CO., LTD.·04719878520508·

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220014·The Hand of Hope (HOH) is a therapy device (exo...

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220090·The Hand of Hope (HOH) is a therapy device (exo...

Puriblood

FDA UDI
PURIBLOOD MEDICAL CO., LTD.·04719878520461·

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220113·The Hand of Hope (HOH) is a therapy device (exo...

Puriblood

FDA UDI
PURIBLOOD MEDICAL CO., LTD.·04719878520492·

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220052·The Hand of Hope (HOH) is a therapy device (exo...

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220083·The Hand of Hope (HOH) is a therapy device (exo...

Puriblood

FDA UDI
PURIBLOOD MEDICAL CO., LTD.·04719878520515·

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220106·The Hand of Hope (HOH) is a therapy device (exo...

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220021·The Hand of Hope (HOH) is a therapy device (exo...

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220038·The Hand of Hope (HOH) is a therapy device (exo...

Puriblood

FDA UDI
PURIBLOOD MEDICAL CO., LTD.·04719878520478·

Puriblood

FDA UDI
PURIBLOOD MEDICAL CO., LTD.·04719878520003·

Puriblood

FDA UDI
PURIBLOOD MEDICAL CO., LTD.·04719878520485·

CLASSIC PLUS METZENBAUM SCISSOR

FDA Adverse Event
Malfunction ·SYMMETRY SURGICAL INC.·Product code LRW·July 30, 2015

IRIS SCISSOR(#130-S), HEMOSTAT MOSQUITO(#161)

FDA Adverse Event
Injury ·MARYAM TRADING·Product code LRW·March 22, 2012

3.4MM MICRO SCISSOR PUNCH

FDA Adverse Event
Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code LRW·February 3, 2009

SWITCH-BLADE SCISSORS, DISPOSABLE

FDA Adverse Event
Malfunction ·CARDINAL HEALTH·Product code LRW·February 4, 2009

KELLY GUM SCS 6-1/4 CV SH

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code LRW·June 2, 2014