137 results · 24ms · Sources: EU EUDAMED, US FDA

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Natrelle 133S Tissue Expander

FDA 510(k)
FDA Unclassified ·Unknown

N/A

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994185129·CASE 9182054 TEMPLTS AND INSERTRS TRAY

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613017712·K-Wire, Double Ended, Trocar Point, Diameter Si...

Bernafon

FDA UDI
Bernafon AG·05711584077214·AQ CO7 B 105, 2.4G NFM DPB SABE/MAC ACCUQ

BOSS Instruments

FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515026230·Deaver Retractor, 10mm, 8"

V200 VENTILATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

GYRUS ACMI PLASMAKINETIC (PK) SUPERPULSE SYSTEM, MODEL 744000 AND DUAL FOOTSWITCH CONNECTOR CABLE, MODEL 710003

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

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·November 7, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 29, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 26, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021