40 results · 19ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

SR1 T3 UPTAKE ENZYME IMMUNOASSAY(MAG SOLID-PHASE)

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450201169·

Pinnacle

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730010421·Pinnacle .018 R UR 4/5 HK -7T 0A 2DO (10PK)

Votion

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730008596·Votion .018 R UR 4/5 HK -7T 0A 2DO (10PK)

Votion®

FDA UDI
Ortho Organizers, Inc.·00190707114299·Votion .018 R UR 4/5 HK -7T 0A 2DO (10PK)

Pinnacle®

FDA UDI
Ortho Organizers, Inc.·00190707112387·Pinnacle .018 R UR 4/5 HK -7T 0A 2DO (10PK)

MODEL 2000 AXYALOOP SELF-TAPPING BONE ANCHOR, MODEL 2000

FDA 510(k)
FDA Class 2 ·Orthopedic

MOBILETT MIRA

FDA 510(k)
FDA Class 2 ·Radiology

InterFuse L

FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010717·Intervertebral Body Fusion Device

InterFuse L

FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010700·Intervertebral Body Fusion Device

InterFuse L

FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010861·Intervertebral Body Fusion Device

InterFuse L

FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010878·Intervertebral Body Fusion Device

InterFuse L

FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010885·Intervertebral Body Fusion Device

InterFuse L

FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010854·Intervertebral Body Fusion Device

InterFuse L

FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010694·Intervertebral Body Fusion Device

InterFuse L

FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010724·Intervertebral Body Fusion Device

FREELITE HUMAN KAPPA AND HUMAN LAMBDA FREE KITS FOR USE ON THE HITACHI 911/912 ANALYZER

FDA 510(k)
FDA Class 2 ·Immunology

HUMAN IGG SUBCLASS LIQUID REAGENT KITS (FOR USE ON HITACHI 911/ 912/ 917 AND MODULAR P)

FDA 510(k)
FDA Class 2 ·Immunology

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORP.·Product code LZG·November 24, 2010

ENDOTAK RELIANCE

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code NVY·January 11, 2013