20 results
·
44ms
·
Sources: EU EUDAMED, US FDA
SKYN SUPREME FEEL EXTRA LUBRICATED
FDA registration
SURETEX, LTD.·1 product·🇹🇭 Thailand
45 Micron Polyisoprene Condom
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Condom, Synthetic
FDA classification
FDA Class 2
·Condom, Synthetic
CS-7
FDA registration
KONICA MINOLTA TECHNOPRODUCTS CO., LTD.·2 products·🇯🇵 Japan
CS-7
FDA registration
KONICA MINOLTA, INC.·2 products·🇯🇵 Japan
CS-7
FDA registration
KONICA MINOLTA, INC.·2 products·🇯🇵 Japan
JO Cumplay Lubricant 8oz (40115)
FDA registration
CC WELLNESS LLC·1 product·🇺🇸 United States
Polyclonal Rabbit Anti-Human IgG/FITC
FDA registration
Agilent Technologies Singapore (International) Pte Ltd.·1 product·🇸🇬 Singapore
Polyclonal Rabbit Anti-Human IgG/FITC
FDA registration
Agilent Technologies Inc.·1 product·🇺🇸 United States
Polyclonal Rabbit Anti-Human IgG/FITC
FDA registration
ATSI Logistics Center ApS·1 product·🇩🇰 Denmark
Polyclonal Rabbit Anti-Human IgG/FITC
FDA registration
Agilent Technologies Denmark ApS·1 product·🇩🇰 Denmark
2008T HEMODIALYSIS MACHINE WITH OPTIONAL CRIT-LINE MONITOR (CLIC)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MED2000 SPA NEBULIZER COMPRESSORS, MODELS P1 AND P2, WITH NEBULIZER, AND MED2000 SPA NEBULIZER, MODEL A1/C (ANDYFLOW)
FDA 510(k)
FDA Class 2
·Anesthesiology
Axoguard HA+ Nerve Protector
FDA UDI
AXOGEN CORPORATION·00850828007121·Axoguard HA+ Nerve Protector is provided steril...
Axoguard HA+ Nerve Protector
FDA UDI
AXOGEN CORPORATION·00850828007145·Axoguard HA+ Nerve Protector is provided steril...
Axoguard HA+ Nerve Protector
FDA UDI
AXOGEN CORPORATION·00850828007114·Axoguard HA+ Nerve Protector is provided steril...
Axoguard HA+ Nerve Protector
FDA UDI
AXOGEN CORPORATION·00850828007138·Axoguard HA+ Nerve Protector is provided steril...
Axoguard HA+ Nerve Protector
FDA UDI
AXOGEN CORPORATION·00850828007107·Axoguard HA+ Nerve Protector is provided steril...
Dialyzer, High Permeability With Or Without Sealed Dialysate System
FDA classification
FDA Class 2
·Dialyzer, High Permeability With Or Without Sealed Dialysate System
Nebulizer (Direct Patient Interface)
FDA classification
FDA Class 2
·Nebulizer (Direct Patient Interface)