582 results · 48ms · 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