1,819 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LensHooke X QC Video (For Semen)
FDA UDI
BONRAYBIO CO., LTD.·04719874741051·
LensHooke X QC Video (For Semen)
FDA UDI
BONRAYBIO CO., LTD.·04719874741044·
LensHooke X QC Video (For Semen)
FDA UDI
BONRAYBIO CO., LTD.·04719874741037·
LensHooke X QC Video (For Semen)
FDA UDI
BONRAYBIO CO., LTD.·04719874741082·
LensHooke X QC Video (For Semen)
FDA UDI
BONRAYBIO CO., LTD.·04719874741099·
OPTILUME BPH CATHETER SYSTEM
FDA Adverse Event
Injury
·UROTRONIC INC.·Product code QXB·September 6, 2024
OPTILUME BPH CATHETER SYSTEM
FDA Adverse Event
Injury
·UROTRONIC INC.·Product code QXB·July 29, 2024
OPTILUME BPH CATHETER SYSTEM
FDA Adverse Event
Injury
·UROTRONIC INC.·Product code QXB·August 2, 2024
OPTILUME BPH CATHETER SYSTEM
FDA Adverse Event
Injury
·UROTRONIC INC.·Product code QXB·December 11, 2024
OPTILUME BPH CATHETER SYSTEM
FDA Adverse Event
Malfunction
·UROTRONIC INC / LABORIE MEDICAL TECHNOLOGIES CORP.·Product code QXB·May 26, 2026
OPTILUME PROCEDURE
FDA Adverse Event
Injury
·LABORIE/UROTRONIC INC·Product code QXB·June 12, 2025
OPTILUME BPH CATHETER SYSTEM
FDA Adverse Event
Injury
·UROTRONIC INC.·Product code QXB·January 3, 2025
OPTILUME BPH CATHETER SYSTEM
FDA Adverse Event
Malfunction
·UROTRONIC INC.·Product code QXB·March 18, 2025
Drug Coated Prostatic Dilation Catheter For Benign Prostatic Hyperplasia
FDA classification
FDA Class 3
·Drug Coated Prostatic Dilation Catheter For Benign Prostatic Hyperplasia
CATALYS LASER
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code OOE·July 28, 2023
Non-contact Infrared Thermometer, Models JXB-315, JXB-319, JXB-320, JXB-311
FDA 510(k)
FDA Class 2
·General Hospital
Vasoview 7XB
FDA UDI
MAQUET CARDIOVASCULAR LLC·00607567700369·Vasoview 7XB
Syrebo
FDA UDI
Shanghai SiYi Intelligent Technology Co., Ltd.·06973408900019·The product is suitable for patients with certa...
NCB, FEMUR PLATE, RIGHT, 13 HOLES, 324 MM
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HRS·May 31, 2018
CUE COVID-19 TEST FOR HOME AND OVER THE COUNTER (OTC) USE
FDA Adverse Event
Malfunction
·CUE HEALTH INC.·Product code QJR·September 6, 2023