611 results · 19ms · Sources: EU EUDAMED, US FDA

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Maquet Getinge-BEQ-TOP 38300 ADULT CPS QID Material: 701055862

FDA Recall
Terminated ·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019

Maquet Getinge BEQ-TOP 38300 ADULT CPS QID Material:701055862R01

FDA Recall
Terminated ·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019

Maquet Getinge-BEQ-TOP 25500 ECC 3/8 w/QiD Material: 701052461

FDA Recall
Terminated ·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019

Maquet Getinge-BEQ-TOP 25503 TMC with BB & QiD Pedi Material:709000473

FDA Recall
Terminated ·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019

Maquet Getinge BEQ-TOP 38300 ADULT CPS QID Material:701055862R01

FDA Enforcement
Class II ·Terminated·Maquet Cardiovascular, LLC·June 5, 2019

Maquet Getinge-BEQ-TOP 38300 ADULT CPS QID Material: 701055862

FDA Enforcement
Class II ·Terminated·Maquet Cardiovascular, LLC·June 5, 2019

BEQ-TOP 25500 ECC 3/8 w/QiD, Custom Tubing Kit, Catalog No. 701052461

FDA Recall
Terminated ·Datascope Corporation·Product code DTN·October 19, 2017

Maquet Getinge-BEQ-TOP 25500 ECC 3/8 w/QiD Material: 701052461

FDA Enforcement
Class II ·Terminated·Maquet Cardiovascular, LLC·June 5, 2019

Maquet Getinge-BEQ-TOP 25503 TMC ¿ with BB & QiD Pedi Material:709000473

FDA Enforcement
Class II ·Terminated·Maquet Cardiovascular, LLC·June 5, 2019

MediSense Precision QID Blood Glucose Test Strips. The product is sold in box of 50 and 100. The NDC number for the 50 count box is 57599-7400-4. The NDC number for the 100 count box is 57599-7401-5.

FDA Recall
Terminated ·AmeriSource Bergen·Product code CGA·January 30, 2004

BEQ-TOP 25500 ECC 3/8 w/QiD, Custom Tubing Kit, Catalog No. 701052461

FDA Enforcement
Class II ·Terminated·Datascope Corporation·May 16, 2018

Bigger-Better-Bladder With 3/8" ID tubing, ITEM BBB38

FDA Recall
Terminated ·Circulatory Technology Inc·Product code DTN·March 3, 2016

Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A Labeled in part: ONE SET - SINGLE USE CATALOG NO. 8002A PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx42'' 1-PRESSURE GAGE LINE 1-PATIENT HOSE 22mmIDx6'' 1-EXHALATION VALVE w/HOLDING ARM& COLLECTION HEAD 48'' w/CUFF 1/4''ID 1-ADULT PRESSURE TEE w/CUFF 1-EXHALATION VALVE LINE 1/8''IDx48'' 2-ADAPTERS 22mmx22mm

FDA Recall
Terminated ·Bio-Med Devices, Inc.·Product code CBK·December 6, 2004

Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A-7 Labeled in part: ONE SET - SINGLE USE ATALOG NO. 8002A-7 PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx60'' 1-EXHALATION VALVE LINE 1/8''IDx90'' 1-PATIENT HOSE 22mmIDx18'' 1-PATIENT HOSE 22mmIDx6'' 1-PRESSURE GAGE LINE 84'' w/CUFF 1/4''ID 1-EXHALATION VALVE w/HOLDING ARM& COLLECTION HEAD 1-ADULT PRESSURE TEE w/CUFF 3-ADAPTERS 22mmx22mm

FDA Recall
Terminated ·Bio-Med Devices, Inc.·Product code CBK·December 6, 2004

Bio Med Devices Patient Breathing Circuit Catalog Number: 80011 Labeled in part: '':PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx42'' 1-PRESSURE GAGE LINE 3/16''IDx54'' 1-PATIENT HOSE 22mmIDx24'' 3-ADAPTERS 22mm x 22mm 1-PATIENT HOSE 22mmIDx6'' 1-ADULT PRESSURE TEE 1-EXHALATION VALVE w/HOLDING ARM& 1-TEMPERATURE ADAPTER 22mmID x 22mm COLLECTION HEAD 2-CUFF 1/4''ID x 5/4'' 1-EXHALATION VALVE LINE 1/8''IDx52''

FDA Recall
Terminated ·Bio-Med Devices, Inc.·Product code CBK·December 6, 2004

Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A-9 Labeled in part: ONE SET - SINGLE USE CATALOG NO. 8002A-9 PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx60'' 1-EXHALATION VALVE LINE 1/8''IDx108'' 1-PATIENT HOSE 22mmIDx36'' 1-PATIENT HOSE 22mmIDx6'' 1-PRESSURE GAGE LINE 1-EXHALATION VALVE w/HOLDING ARM&COLLECTION HEAD 102'' w/CUFF 1/4''ID 1-ADULT PRESSURE TEE w/CUFF 3-ADAPTERS 22mmx22mm

FDA Recall
Terminated ·Bio-Med Devices, Inc.·Product code CBK·December 6, 2004

Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2412 ( 2 x 12 channel)

FDA Recall
Terminated ·QiG Group LLC·Product code LGW·January 26, 2016

Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8 channel)

FDA Recall
Terminated ·QiG Group LLC·Product code LGW·January 26, 2016

Algostim LLC, Algovita External Pulse Generator, Trial Stimulator, Model 3400

FDA Recall
Terminated ·QiG Group LLC·Product code LGW·January 26, 2016

Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8 channel)

FDA Enforcement
Class II ·Terminated·QiG Group LLC·March 30, 2016