10,000 results
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42ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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JUD care
FDA UDI
Shenzhen Juding Medical Co., Ltd.·06973495370085·Portable Sampling Booth-Consumables: Purificati...
Saneso Lens Wash Bottle Assembly (SAN-LWB-A)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
I-STAT TROPONIN (HS-TNI ) CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code MMI·May 13, 2026
I-STAT CG8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·January 25, 2022
I-STAT TROPONIN (HS-TNI ) CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code MMI·May 20, 2026
I-STAT TROPONIN (HS-TNI ) CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code MMI·April 22, 2026
AMPHETAMINES LOW
FDA UDI
UTAK LABORATORIES, INC.·B800AMPHLWBFTDPS0·AMPHETAMINES LOW
I-STAT TROPONIN (HS-TNI ) CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code MMI·May 13, 2026
ENDOSSEOUS DENTAL IMPLANT
FDA Adverse Event
Injury
·STRAUMANN MANUFACTURING, INC.·Product code DZE·July 22, 2022
I-STAT CG8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·August 25, 2020
I-STAT CG8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·September 6, 2018
I-STAT CG8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·February 8, 2022
I-STAT CG8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·February 8, 2022
I-STAT CG8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·September 28, 2020
I-STAT TROPONIN (HS-TNL) CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE INC.·Product code MMI·August 27, 2025
I-STAT B-HCG CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code DHA·July 30, 2024
Stimulator, Functional Neuromuscular, Scoliosis
FDA classification
FDA Class 3
·Stimulator, Functional Neuromuscular, Scoliosis
Lab
FDA UDI
STERNGOLD DENTAL LLC·00841549115868·Lab Burnout Post Starter Kit
RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R
FDA 510(k)
FDA Class 2
·Neurology
RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL
FDA 510(k)
FDA Class 2
·Neurology