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Perc

FDA UDI
Smith & Nephew, Inc.·00817470003444·SPINE NEEDLE,17 GAUGE CRAWFORD, 6 ...

Spine Needle and Cannula

FDA UDI
MORGAN STEER ORTHOPAEDICS LIMITED·05060696460064·Crawford 17 ga x 6” cannula (x10)

Spine Needle and Cannula

FDA UDI
MORGAN STEER ORTHOPAEDICS LIMITED·05060696460071·DC 19 ga x 3” Cannula (10)

Perc

FDA UDI
Smith & Nephew, Inc.·00817470003468·PERC-DC 19 GAUGE 4IN TROCAR NEEDLE 10

ARROW

FDA UDI
TELEFLEX INCORPORATED·00801902076847·Continuous Peripheral Nerve Block Kit with Non-...

ARROW

FDA UDI
TELEFLEX INCORPORATED·00801902076861·Continuous Peripheral Nerve Block Kit with Non-...

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780153788·Integra® Jarit® Knurled Sleeve Only For #'s 290...

Keenhealth

FDA UDI
Sevenground Trading B.V.·08719699632714·K-NS-356-60 is a better breath Stop Snoring Nas...

Keenhealth

FDA UDI
Sevenground Trading B.V.·08719699632448·K-NS-356 is a better breath Stop Snoring Nasal ...

DUETTE MULTI-BAND MUCOSECTOMY DEVICE

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code KNS·April 2, 2020

DREAMTOME¿ RX 44

FDA Adverse Event
Malfunction ·Product code KNS·July 30, 2018

DUETTE MULTI-BAND MUCOSECTOMY DEVICE

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code KNS·April 2, 2020

EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·May 28, 2026

ACTIVA

FDA Adverse Event
Injury ·IPG MFG SWITZERLAND·Product code MHY·November 21, 2014

ACTIVA

FDA Adverse Event
Injury ·IPG MFG SWITZERLAND·Product code MHY·November 21, 2014

EVIS EXERA III COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·September 19, 2024

EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·March 4, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 25, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 21, 2024