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

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COLLEAGUE CX VOLUMETRIC INFUSION PUMP 2M8161 AND VOLUMETERIC INFUSION PUMP 2M8151

FDA 510(k)
FDA Class 2 ·General Hospital

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00202111·

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00272111·

SoftTip® medium

FDA UDI
Honeywell Healthcare Solutions GmbH·04036616010016·SoftTip® medium RM-3212-9 MySign® FDA

L1-M-002211

Basic UDI-DI
EU MDD · Eu Md Class 2a ·Ze Fang Technology Co., Ltd.·1 device

BetaForce™

FDA UDI
Ortho Organizers, Inc.·00190707124571·BETAFORCE Beta³ Lower 19x25 (10pk)

BetaForce

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730022189·Beta3 Lower 19x25 10 archwires per pack

XIPHOS ZFUZE

FDA UDI
Difusion Technologies, Inc.·00853896008007·PLIF Spacer 22mm Long x 11mm Height

Battalion

FDA UDI
ALPHATEC SPINE, INC.·00840967188706·Battalion, LLIF Trial, 0°, 22 mm Wide, 11 mm X ...

MODIFICATION TO INTRALASE 600C LASER KERATOME

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

BUILD-IT FR

FDA 510(k)
FDA Class 2 ·Dental

INTACS PRESCRIPTION INSERTS

FDA Adverse Event
Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

STEM: AMISTEM P AMISTEM- P SHORT NECK STD STEM SIZE 3

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 25, 2021

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code OYC·March 13, 2013

CE MULTIRATE INFUSOR LV2,3,512 PACK

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 28, 2011

UNK DEPUY PRODUCT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HWC·February 21, 2008

INTACS PRESCRIPTION INSERTS

FDA Adverse Event
Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code NHL·February 16, 2026

SYRINGE 50ML LL

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 21, 2020

INTACS CORNEAL IMPLANTS

FDA Adverse Event
Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006