31 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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ATRICLIP LAA EXCLUSION SYSTEM WITH PRELOADED GILLINOV-COSGROVE CLIP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Impact™
FDA UDI
B BRAUN INTERVENTIONAL SYSTEMS, INC·04046964290763·IMPACT BALLOON CATHETER 14MMX2CMX120CM
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192909·12mm X 100mm Stem Pilot
IV Administration Set
FDA UDI
B. BRAUN MEDICAL INC.·04046964188251·Primary Gravity IV Set, 2 Non-Needle-Free Injec...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197043700·Ewald Hudson Tissue Forceps
12.0cm...
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973101499·Poly Insert MPCS, Size 1L, 20mm
Chic
FDA UDI
Gc Orthodontics America Inc.·E53514212000101·CHIC ROTH 022/UR2 8T 9A 0OF
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197477338·Denhart mouth gag
120mm,...
Chic
FDA UDI
Gc Orthodontics America Inc.·E53514212000201·CHIC MBT 022/UR2 10T 8A
Chic
FDA UDI
Gc Orthodontics America Inc.·D78814212000201·CHIC MBT 022/UR2 10T 8A
Chic
FDA UDI
Gc Orthodontics America Inc.·D78814212000101·CHIC ROTH 022/UR2 8T 9A 0OF
ONE TOUCH BASIC ENHANCED
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·November 8, 2001
NIPPV SILICONE FACE MASK, NIPPV ECONOMY FACE MASK, NIPPV SILICONE NASAL MASK MODEL 10212, 10222, 10202
FDA 510(k)
FDA Class 2
·Anesthesiology
POWDERED VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
SYRINGE 5ML SALINE FILL CHINA SP
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code NGT·June 11, 2025
EARLYVUE VS30
FDA Adverse Event
Malfunction
·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code DQA·February 19, 2026
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 4, 2014
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTN·June 3, 2013
ON-Q PAINBUSTER INTL
FDA Adverse Event
Malfunction
·I-FLOW CORP.·Product code MEB·May 26, 2011
BD PHOENIX PMIC110
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·October 19, 2021