5,943 results
·
39ms
·
Sources: EU EUDAMED, US FDA
GARMENT, PROTECTIVE, FOR INCONTINENCE
FDA registration
JIANGSU NEW PENTASTAR MEDICAL PRODUCTS CO. LTD.·1 product·🇨🇳 China
PACK, HOT OR COLD, DISPOSABLE
FDA registration
JIANGSU NEW PENTASTAR MEDICAL PRODUCTS CO. LTD.·1 product·🇨🇳 China
System, Blood Collection, Vacuum-Assisted, Manual - Blood Collection Needle Holder
FDA registration
JIANGSU NEW PENTASTAR MEDICAL PRODUCTS CO. LTD.·1 product·🇨🇳 China
STOCKING, MEDICAL SUPPORT (TO PREVENT POOLING OF BLOOD IN LEGS)
FDA registration
JIANGSU NEW PENTASTAR MEDICAL PRODUCTS CO. LTD.·1 product·🇨🇳 China
Urinary drainage collection kit, for indwelling catheter
FDA registration
JIANGSU NEW PENTASTAR MEDICAL PRODUCTS CO. LTD.·1 product·🇨🇳 China
BF2M20S8A
FDA UDI
KOVEN TECHNOLOGY, INC.·00894912002289·2 MHz flat CW Doppler probe.
LED Facial Mask with Ice compress
FDA registration
SHENZHEN WILLCAREYOU TECHNOLOGY CO., LTD·2 products·🇨🇳 China
Rehabilitation Robot Gloves RRG-300, RRG-310, RRG-320, RRG-330, RRG-330N, RRG-400
FDA registration
SHENZHEN WILLCAREYOU TECHNOLOGY CO., LTD·1 product·🇨🇳 China
Laser Hair Growth Cap
FDA registration
SHENZHEN WILLCAREYOU TECHNOLOGY CO., LTD·1 product·🇨🇳 China
Led Light Therapy Foot Machine
FDA registration
SHENZHEN WILLCAREYOU TECHNOLOGY CO., LTD·1 product·🇨🇳 China
L38xi/10-5 MHz Armored
Device
EU MDR
·
Eu Md Class 2a
·Fujifilm Sonosite, Inc.·Not intended for eu market
rP19x/5-1 MHz Armored
Device
EU MDR
·
Eu Md Class 2a
·Fujifilm Sonosite, Inc.·Not intended for eu market
rC60xi/5-2 MHz Armored
Device
EU MDR
·
Eu Md Class 2a
·Fujifilm Sonosite, Inc.·Not intended for eu market
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·AcrySof ReSTOR Posterior Chamber Intraocular Lenses
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Clareon Aspheric Hydrophobic Acrylic Intraocular Lens (with the AutonoMe Pre-Loaded Delivery System) Claeron Toric Asphe
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·AcrySof Posterior Chamber Intraocular Lens
Arrow 0.2 Micron Flat Filter, GVS
FDA 510(k)
FDA Class 2
·Anesthesiology
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MODEL 9790C PROGRAMMER AND MODEL 9891 PE SOFTWARE
6.0 MHZ LA6060 TRANSDUCER & 4.0 MHZ LA4011 TRANSDU
FDA 510(k)
FDA Class 2
·Radiology
REFAGO
FDA UDI
Shenzhen Kairuigeli Investment Consultant Co., Ltd.·06970649350115·