13 results
·
62ms
·
Sources: EU EUDAMED, US FDA
DR. JAPAN CO., LTD.
FDA registration
DR. JAPAN CO., LTD.·2 products·🇯🇵 Japan
RELI QUINCKE POINT SPINAL NEEDLE
FDA Adverse Event
Malfunction
·DR. JAPAN CO., LTD.·Product code BSP·October 5, 2016
MCKESSON
FDA Adverse Event
Malfunction
·DR. JAPAN CO. LTD.·Product code BSP·October 20, 2017
RELI
FDA Adverse Event
Malfunction
·DR. JAPAN CO., LTD.·Product code BSP·December 5, 2020
RELI
FDA Adverse Event
Injury
·DR, JAPAN CO., LTD.·Product code BSP·July 16, 2025
RELI QUINCKE POINT SPINAL NEEDLE
FDA Adverse Event
Malfunction
·DR. JAPAN CO. LTD.·Product code BSP·March 22, 2017
ACCUTIP
FDA Adverse Event
Malfunction
·DR. JAPAN CO. LTD.·Product code BSP·March 11, 2019
SELECT
FDA Adverse Event
Malfunction
·DR. JAPAN CO. LTD.·Product code BSP·October 5, 2016
RELI QUINCKE POINT SPINAL NEEDLE
FDA Adverse Event
Malfunction
·DR. JAPAN CO. LTD.·Product code BSP·August 30, 2016
RELI QUINCKE POINT SPINAL NEEDLE
FDA Adverse Event
Malfunction
·DR. JAPAN CO., LTD.·Product code BSP·April 18, 2017
ACCUTIP
FDA Adverse Event
Injury
·DR. JAPAN CO. LTD.·Product code BSP·October 29, 2019
CS100 INTRA-AORTIC BALLOON PUMP, JAPANESE, 110V
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·July 15, 2022
KHANG BAO INTERNATIONAL KFT
Authorized representative
🇭🇺 Hungary·119 Manufacturers·1262 Devices