58 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SPECTRUM SILICONE FOLEY CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756000109·Cervical Collar
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964002562·The ENDO CARRY-ON Procedure Kit contains all of...
NEW METAL STRIPS
FDA UDI
Gc America Inc.·14548161391610·NEW METAL STRIPS Assortment "A" Package, #200 M...
NEW METAL STRIPS
FDA UDI
Gc America Inc.·D0470002511·NEW METAL STRIPS Assortment "A" Package, #200 M...
intellijoint HIP®
FDA UDI
Intellijoint Surgical Inc·00628184002513·Camera, G2
ULTRAPAK CAT. #100-0251
FDA 510(k)
FDA Class 1
·Hematology
LIFEPAK® 12 defibrillator/monitor
FDA UDI
PHYSIO-CONTROL, INC.·00721902399572·LP12AABBBBAABABBAABAAAAALP12 MONITOR-DEFIB
Electrode
FDA UDI
I.C. MEDICAL, INC.·00817688020974·
QB1 NMES SYSTEM, BILATERAL, SMALL/MEDIUM
FDA UDI
Motive Health, Inc.·00854691008698·QB1 NMES SYSTEM, BILATERAL, SMALL/MEDIUM
e-vive BILATERAL NMES SYSTEM; SMALL / MEDIUM (2.0 Dock)
FDA UDI
Motive Health, Inc.·00854691008537·e-vive BILATERAL NMES SYSTEM; SMALL / MEDIUM (...
PERRY-KOLBERG (PK) HA-COATED TITANIUM SLEEVE
FDA 510(k)
FDA Class 2
·Ophthalmic
ACTICOAT FOAM DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
Central Venous Catheter Kit
FDA UDI
BIOPTIMAL INTERNATIONAL PTE. LTD.·08886483508859·
8900-000251-05
FDA Adverse Event
Malfunction
·BIO-DETEK INCORPORATED·Product code MKJ·December 5, 2023
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code JTC·February 1, 2000
CM ALVIM IMPLANT 3.5X11.5
FDA Adverse Event
Injury
·NEODENT - JJGC S.A.·Product code DZE·November 9, 2017
TMJ SMALL RIGHT FOSSA
FDA Adverse Event
BIOMET MICROFIXATION·Product code LZD·March 16, 2010
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·March 12, 2013
GYNNIE OB-GYN STRETCHER
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code HDD·February 3, 2011