10,000 results
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66ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544012863·Instrument, Quad Driver, Long
NA
FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544012870·Instrument, Quad Driver, Medium
NA
FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544012887·Instrument, Quad Driver, Short
FREE STYLE LIBRE 14 DAY GLUCOSE INVASIVE
FDA Adverse Event
Injury
·ABBOTT DIABETES CARE, INC.·Product code MDS·June 26, 2019
PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER
FDA Adverse Event
Injury
·COOK INCORPORATED·Product code DQO·December 27, 2007
EVA VITRECTOMY TDC KIT 2-STEP 23G
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER INT.·Product code QDY·February 9, 2023
EVA VITRECTOMY PACK GRAVITY INPUT 25G
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code QDY·March 30, 2023
EVA TDC VITRECTOMY PACK VGPC INPUT 25G
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code QDY·January 4, 2019
EXTENDIBLE BRUSH BACKFLUSH INSTRUMENT WITH ACTIVE
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code QDY·February 22, 2019
EVA TDC VITRECTOMY PACK VGPC INPUT 25G
FDA Adverse Event
Injury
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code QDY·January 11, 2019
EXTENDIBLE BRUSH BACKFLUSH INSTRUMENT WITH ACTIVE
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code QDY·February 22, 2019
EVA TDC VITRECTOMY PACK GRAVITY INPUT 25G
FDA Adverse Event
Injury
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code QDY·January 11, 2019
EVA TDC VITRECTOMY PACK VGPC INPUT 25G
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code QDY·January 4, 2019
EVA TDC VITRECTOMY PACK VGPC INPUT 25G
FDA Adverse Event
Malfunction
·D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNA·Product code QDY·January 4, 2019
Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Number: USA-LPH024
FDA Recall
Terminated
·Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom·Product code QDI·January 18, 2022
Vitrectomy Kit
FDA classification
FDA Class 2
·Vitrectomy Kit
Fish Based Detection Of Chromosomal Abnormalities From Patients With Hematologic Malignancies
FDA classification
FDA Class 2
·Fish Based Detection Of Chromosomal Abnormalities From Patients With Hematologic Malignancies
HDI INC.
FDA registration
HDI INC.·18 products·🇰🇷 South Korea
IDIS CO., LTD.
FDA registration
IDIS CO., LTD.·2 products·🇰🇷 South Korea
Acera Surgical - Adie Road
FDA registration
Acera Surgical - Adie Road·1 product·🇺🇸 United States