37 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
STANDARD IMAGING HDR 1000 PLUS ION CHAMBER; STANDARD IMAGING IVB 1000 ION CHAMBER
FDA 510(k)
FDA Class 2
·Radiology
MySign® O
FDA UDI
Honeywell Healthcare Solutions GmbH·04036616009324·MySign® O incl. OOM111
Scanlan® SURG-I-BAND® color coding
FDA UDI
SCANLAN INTERNATIONAL INC·00846159001808·Scanlan® SURG-I-BAND® color coding - Labels-Jam...
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756814935·ADULT 60 In CORRUGATED CIRCUIT
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361008798·Pedicle Screw Assy. Cann REset Ø5x25mm
NA
FDA UDI
aap Implantate AG·04042409048173·K-wire with trocar point, ø1.8, L 250
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197522489·TV-adapter 4k
f=28mm...
LIFECARD CF COMPACT RECORDER
FDA 510(k)
FDA Class 2
·Cardiovascular
4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
aap Implantate AG·04042409048180·K-wire with trocar point, ø1.8, L 250
MaxTorque™
FDA UDI
TORNIER, INC.·00846832054251·
PREMIUM PLUS CEEA
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code GDW·April 19, 2018
TUFF UNICON IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 27, 2026
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·March 13, 2013
PROSTAR XL SUTURE-MEDIATED CLOSURE
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·February 25, 2011
DIAPACT CRRT KIT
FDA Adverse Event
Other
·B. BRAUN MEDICAL, INC.·Product code FII·January 23, 2008
BIOMET CC I-BEAM TRAY 71MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018
VANGUARD PS TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·January 2, 2019
M2A TAPER LINER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·October 10, 2017
COMPREHENSIVE SHOULDER SYSTEM NANO HUMERAL COMP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSD·September 26, 2023