582 results
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48ms
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Sources: EU EUDAMED, US FDA
Needle (various)
FDA registration
BOULDER BIOMED LLC·1 product·🇺🇸 United States
iMap 3d Mapping and Navigation System
FDA registration
BOULDER BIOMED LLC·1 product·🇺🇸 United States
Accu-joint Hemi Implant Single Sterile
FDA registration
BOULDER BIOMED LLC·1 product·🇺🇸 United States
MB-Series Single-Use Cerebrovascular Flowprobe
FDA registration
BOULDER BIOMED LLC·1 product·🇺🇸 United States
BOULDER BIOMED LLC
FDA registration
BOULDER BIOMED LLC·2 products·🇺🇸 United States
WORK HARDENING,SYSTEM II w/8920
FDA UDI
Hausmann Enterprises, LLC·00840314806499·
Quadrox iD w RF 32 Pack
FDA UDI
DATASCOPE CORP.·00607567205758·BO-HMOD 70000-USA Adult Quadrox iD,
BO-RF32 Rot...
KIT, DUPEL II, w/SAFETY SOCKET
FDA UDI
EMPI, INC.·00888912151375·
0800,APS0,08,AV,N,LT,ICW
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828153294·0800,APS0,08,AV,N,LT,ICW
IQ PRODUCTS TRIPLE-COLOR FLOW CYTOMETRY REAGENTS, IQ PRODUCTS CD45-FITC/CD4-PE/CD3-CYQ, IQ PRODUCTS CD45-FITC/CD8-PE/CDQ
FDA 510(k)
FDA Class 2
·Hematology
Nuewa I9T/Nuewa I9 Exp/Nuewa I9 Easi/Anesus I9 Diagnostic Ultrasound System
FDA registration
Shenzhen Mindray Bio-Medical Electronics Co.,LTD·3 products·🇨🇳 China
Nuewa I9T/Nuewa I9 Exp/Nuewa I9 Easi/Anesus I9 Diagnostic Ultrasound System
FDA registration
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD.·3 products·🇨🇳 China
NA
FDA UDI
NIHON KOHDEN AMERICA, INC.·00841983103896·PAPER for BSM-2/4/5000+ CNS
NA
FDA UDI
NIHON KOHDEN AMERICA, INC.·00841983103889·PAPER for BSM-6000
Vermed
FDA UDI
GRAPHIC CONTROLS ACQUISITION CORP·00009336000982·Electrocardiographic recording paper
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Prospera Spinal Cord Stimulation (SCS) System, Resilience Percutaneous Lead, HomeStream Remote Management
VARICELLA-ZOSTER(IGG) IFA TEST
FDA 510(k)
FDA Class 2
·Microbiology
GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP
FDA 510(k)
FDA Class 2
·Ophthalmic
DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000
FDA 510(k)
FDA Class 2
·Microbiology
VIRO VARICELLA-ZOSTER VIRUS IDENTIFICATION REAGENT
FDA 510(k)
FDA Class 2
·Microbiology