24 results · 23ms · Sources: EU EUDAMED, US FDA

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RENASYS TOUCH Negative Pressure Wound Therapy, RENASYS TOUCH Canisters, RENASYS TOUCH Carry Bag, Carry Strap, RENASYS Y-Connector, RENASYS TOUCH IV Pole/Bed Clamp, RENASYS TOUCH Class 2 Power Supply

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Oticon

FDA UDI
Oticon A/S·05707131292131·ALTA2 PRO, BTE 13 WL 105 SIL

Symmetry Hartman

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482035689·Symmetry® Forceps, Hartman Baby Mosquito, Strai...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575364473·Medullary canal orthopaedic reamer, rigid - End...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575364466·Medullary canal orthopaedic reamer, rigid - End...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575364459·Medullary canal orthopaedic reamer, rigid - End...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575364442·Medullary canal orthopaedic reamer, rigid - End...

TANGO+ AUTOMATIC BLOOD PRESSURE AND OXYGEN SATURATION MEASUREMENT SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

VERIGENE RESPIRATORY VIRUS NUCLEIC ACID TEST +(RVNAT+)

FDA 510(k)
FDA Class 2 ·Microbiology

HNM Medical

FDA UDI
HNM STAINLESS, LLC.·00842962111284·BABY HARTMAN MOSQUITO FORCEPS, 3 7/8", STR

BAXJECT II HI-FLOW

FDA Adverse Event
Malfunction ·TAKEDA PHARMACEUTICALS U.S.A INC.·Product code LHI·May 4, 2026

BAXJECT II HI-FLOW

FDA Adverse Event
Malfunction ·TAKEDA PHARMACEUTICALS U.S.A INC.·Product code LHI·May 4, 2026

BAXJECT II HI-FLOW NEEDLESS TRANSFER DEVICE

FDA Adverse Event
Malfunction ·TAKEDA PHARMACEUTICALS U.S.A., INC.·Product code LHI·May 4, 2026

BAXJECT II HI-FLOW NEEDLESS TRANSFER DEVICE

FDA Adverse Event
Malfunction ·TAKEDA PHARMACEUTICALS U.S.A., INC.·Product code LHI·May 4, 2026

BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 26, 2024

ELECTRODE, PACEMAKER, PERMANENT

FDA Adverse Event
Injury ·MPRI·Product code DTB·June 8, 2013

COGNIS

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 7, 2011

RENEGADE? HI-FLO? KIT

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KRA·October 8, 2014

BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 15, 2024

BAXJECT II HI-FLOW

FDA Adverse Event
Malfunction ·TAKEDA PHARMACEUTICALS U.S.A INC.·Product code LHI·May 4, 2026