23 results
·
27ms
·
Sources: EU EUDAMED, US FDA
ATAC CALCIUM REAGENT AND ATAC CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Accolade TMZF Plus Hip Stem: Catalog # 3020-0537 Accolate d TMZF Hip Stem # 5 Catalog #6020-3535 Accolade 132 Size 3.5 Catalog # 6021-0230 Accolade Plus TMZF Hip Stem #2 Catalog # 6021-0335 Accolade Plus TMZF Hip Stem #3 Catalog #3021-0435 Accolade TMZF Hip Stem #4 Catalog # 6021-0435 Accolade Plus TMZF Hip Stem #4 Catalog #6021-2530 Accolade (127 deg) Size 2.5 Accolade (127 deg) Size 2.5 Catalog # 6021-4535 Accolade (127 DEG) Size 4.5 K994366; k023105; K032300 Manufactured by " Stryker Ireland, Carrigtwohill Industrial Estate Carrington County Cork, Ireland The subject hip stem is a single-use device intended for the reconstruction of the head and neck of the femoral joint. This hip stem is intended for primary reconstruction of the proximal femur or revision total hip arthroplasty.
FDA Recall
Terminated
·Stryker Howmedica Osteonics Corp.·Product code ISL·March 1, 2011
Angled Tip
FDA UDI
COOK INCORPORATED·00827002145986·Angled Tip Ureteral Catheter with Bentson PTFE-...
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668113806·VISCO CANNULA 30GA ANGLE 8MM
EasyDrip Plus Pen Needles 31G×5mm
FDA UDI
Sandstone Medical (Suzhou) Inc.·16972857293182·
EasyDrip Plus Pen Needles 31G 5mm
FDA UDI
Sandstone Medical (Suzhou) Inc.·16972857292987·
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00888233025188·
ALLOGENIX
FDA UDI
BIOMET MICROFIXATION, INC·00841036125868·
Reicodent
FDA UDI
devemed GmbH·04061644049066·Wire cutter TC | 11.5 cm
for soft wires up to 0...
Angled Tip
FDA UDI
COOK INCORPORATED·00827002146716·Angled Tip Ureteral Catheter
Arsenal
FDA UDI
ALPHATEC SPINE, INC.·00840967162416·OFFSET THORACIC SUPRALAMINAR HOOK, RIGHT, 10.5mm
FORTAFLEX SURGICAL MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BIOSPHERE MEDICAL INFUSION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
STRYKER CORPORATION·04546540944986·Precision Offset (9.0 x 0.254 x 18.5mm)
GOBED+
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 27, 2013
HEARTSTART MRX -EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·February 15, 2011
COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 3, 2008
UNK_HARMONIC HD1000I
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 30, 2025
FEMALE LL ADAPTOR
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·February 26, 2021
Portex PEEP-KEEP Dual-Axis Swivel Adapter Catalog Number: 525351
FDA Recall
Terminated
·Smiths Medical ASD, Inc.·September 9, 2004