674 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
e.p.t. Early Pregnancy Test
FDA UDI
Nfi Consumer Products·00045611953031·ept analog 3 Ct
e.p.t. Direct
FDA UDI
Nfi Consumer Products·00045611963030·e.p.t. Direct 3 ct.
e.p.t. Direct
FDA UDI
Nfi Consumer Products·00045611962026·e.p.t. Direct 2 ct.
e.p.t. Analog
FDA UDI
Nfi Consumer Products·00045611952027·e.p.t. Analog 2 Ct
KINGSWAY PHARMACEUTICALS DBA NFI, LLC
FDA registration
KINGSWAY PHARMACEUTICALS DBA NFI, LLC·6 products·🇺🇸 United States
BioButton (Reprocessed, NF Version)
FDA UDI
BIOINTELLISENSE, INC.·00850005949565·The BioButton™ is a remote monitoring wearable ...
NOVOPEN 6
FDA Adverse Event
Injury
·NOVO NORDISK A/S·Product code FMF·December 19, 2024
NOVOPEN
FDA Adverse Event
Injury
·NOVO NORDISK A/S·Product code FMF·December 19, 2024
ECHELON*FLEX60 LONG
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 24, 2014
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·February 1, 2018
MW5080358
FDA Adverse Event
Injury
·October 3, 2018
Test, Cocaine And Cocaine Metabolites, Over The Counter
FDA classification
FDA Class 2
·Test, Cocaine And Cocaine Metabolites, Over The Counter
Device, Hardcopy, Images, Ophthalmic
FDA classification
FDA Class 2
·Device, Hardcopy, Images, Ophthalmic
CFI RESTRAINT BELT (CFI-168) / CFI RESTRAINT BELT (CFI-4046)
FDA 510(k)
FDA Class 1
·General Hospital
DFI CO., LTD.
FDA registration
DFI CO., LTD.·10 products·🇰🇷 South Korea
PREMIER OPTICAL MFY. LTD.
FDA registration
PREMIER OPTICAL MFY. LTD.·4 products·🇭🇰 Hong Kong
WAH MING OPTICAL MFY. LTD.
FDA registration
WAH MING OPTICAL MFY. LTD.·3 products·🇭🇰 Hong Kong
LFI-DOWN RETRACTOR
FDA UDI
W.H. Holden, Inc.·D9282007190·
QwikCheck DFI Kit
FDA UDI
M.E.S. MEDICAL ELECTRONIC SYSTEMS LTD.·07290016650617·
FLUID ADMINISTRATIVE SET, AFI
FDA 510(k)
FDA Class 2
·General Hospital