5,205 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DM4
FDA UDI
ZOE MEDICAL INCORPORATED·00851920007330·The DM4 Monitor is intended for monitoring, rec...
0307,APS0,08,N,FW
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828101264·0307,APS0,08,N,FW
DirectView 4 Mirror NF w/ Handle
FDA UDI
Ion Vision, Inc·00850054345493·
DirectView 4 Mirror NF w/ Handle
FDA UDI
Ion Vision, Inc·00850054345370·
BOTTLE,NF W/SAL
FDA Adverse Event
Malfunction
·HAEMONETICS CORPORATION·Product code KSR·February 27, 2023
Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -MFW, -NFW), Model Number 91331
FDA Enforcement
Class II
·Ongoing·Zoe Medical Incorporated·September 18, 2024
SAFE LIFE T-DIP MULTI-DRUG URINE TEST PANEL (10 PANEL)
FDA Adverse Event
Injury
·UNK·Product code NFW·November 17, 2025
Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -MFW, -NFW), Model Number 91331
FDA Recall
Open, Classified
·Zoe Medical Incorporated·Product code DQA·August 13, 2024
Test, Cannabinoid, Over The Counter
FDA classification
FDA Class 2
·Test, Cannabinoid, Over The Counter
HILO TABLES, TYPE CH-4, CH-8, FW-6, FW-5, FW-2, AL
FDA 510(k)
FDA Class 2
·Physical Medicine
BMT Medizintechnik GmbH
FDA UDI
BMT Medizintechnik GmbH·04251725200473·EXPLORER/PROBE GOLDMANN-FOX-WILLIAMS
EFH-7F-W
FDA UDI
BIOTRONIK SE & Co. KG·04035479145323·
EFH-6F-W
FDA UDI
BIOTRONIK SE & Co. KG·04035479157838·
EFH-6F-W
FDA UDI
BIOTRONIK SE & Co. KG·04035479157821·
NEW STETIC
FDA registration
NEW STETIC·13 products·🇨🇴 Colombia
NEW LANTERN
FDA registration
NEW LANTERN·1 product·🇺🇸 United States
BFW, INC.
FDA registration
BFW, INC.·1 product·🇺🇸 United States
MAXENON
FDA Adverse Event
Injury
·BFW·Product code FTD·December 31, 2013
FREESTYLE PRECISION NEO
FDA Adverse Event
Malfunction
·NBW·Product code NBW·January 18, 2018
PRECISION XTRA
FDA Adverse Event
Malfunction
·NBW·Product code NBW·April 28, 2017