38 results · 21ms · Sources: EU EUDAMED, US FDA

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EQUINOXE GLENOID, UHMWPE 16 PS=OSTERIOR AUGMENT PEGGED, SMALL, LEFT/RIGHT

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772813827·GENUMEDI PRO SILVER SIZE II

ATEC 1212-20

FDA UDI
Hologic, Inc.·15420045504912·12G (2.7MM) X 12CM, 20MM HANDPIECE

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776164133·TUNGSTEN CARBIDE MATHIERU NEEDLE HOLDER

DD tempMED

FDA UDI
Dental Direkt GmbH·EDDIK112201·DD tempMED are pre-colored dental milling blank...

TALOS® HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167321212200·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167311212200·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450743751·

Corneal Trephine Blade

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896120235·Corneal Trephine Blade

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780180289·Integra® Jarit® Mathieu Needle Holder, 8", Carb...

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981246495·Interbody, 39mm x 27mm X 12mm, 20 Deg

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981265731·Trial, 39mm x 27mm x 12mm, 20 Deg

ATEC VACUUM ASSISTED BREAST BIOPSY DEVICE

FDA Adverse Event
Other ·HOLOGIC INC. - INTERVENTIONAL BREAST SOLUTIONS DIVISION·Product code KNW·September 5, 2008

NITRILE PATIENT EXAMINATION GLOVE POWDER-FREE (BLUE COLOR) TESTED FOR USE WITH CHEMOTHERAPY DRUGS

FDA 510(k)
FDA Class 1 ·General Hospital

EXPLORER 4D TREATMENT PLANNING SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

ATEC VACUUM ASSISTED BREAST BIOPSY DEVICE

FDA Adverse Event
Other ·HOLOGIC, INC - INTERVENTIONAL BREAST SOLUTIONS DIVISION·Product code KNW·October 3, 2008

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351116933·LAP-Insert only, Ø5mm, l=200mm Grasp....

Experience

FDA UDI
Gc Orthodontics America Inc.·D78812122000101·EXMC ROTH 018/UL2 8T 9A

ATEC 1212-20 HANDPIECE

FDA Adverse Event
Other ·SUROS SURGICAL SYSTEMS, INC.·Product code GDF·February 1, 2007

ATEC BREAST BIOPSY AND EXCISION SYSTEM

FDA Adverse Event
Other ·HOLOGIC, INC.·Product code KNW·August 1, 2011