10,000 results
·
60ms
·
Sources: EU EUDAMED, US FDA
Covidien llc
Manufacturer
🇺🇸 United States·1 Basic UDI-DI·1 Device·2 Importers·TÜV SÜD Product Service GmbH
Argyle
Device
EU MDD
·
Eu Md Class 2a
·Covidien llc·No longer on the market
Covidien LLC
FDA registration
Covidien LLC·20 products·🇺🇸 United States
Covidien llc
FDA registration
Covidien llc·10 products·🇺🇸 United States
Covidien llc
FDA registration
Covidien llc·11 products·🇺🇸 United States
Covidien Medical Products (Shanghai) Manufacturing LLC
FDA registration
Covidien Medical Products (Shanghai) Manufacturing LLC·8 products·🇨🇳 China
GASTRIC LAVAGE KIT SMALL
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Covidien llc·1 device
COVIDIEN LLC ENDO STITCH AUTO SUTURE SUTURING
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GAM·June 9, 2025
COVIDIEN LLC ENDO STITCH AUTO SUTURE SUTURING
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GAM·June 9, 2025
CURITY IODOFORM PACKING STRIP
FDA Adverse Event
Malfunction
·COVIDIEN / CARDINAL HEALTH·Product code EFQ·June 16, 2021
SONICISION
FDA Adverse Event
Malfunction
·COVIDIEN LP·Product code LFL·November 15, 2024
HI LO TRACHEAL TUBE CUFFED / SHILEY HI LOW ORAL NASAL TUBE
FDA Adverse Event
Injury
·Product code BTR·September 25, 2020
MONOJECT 3 ML SYRINGE WITH STANDARD HYPODERMIC NEEDLE 23GX1"
FDA Adverse Event
Malfunction
·COVIDIEN/CARDINAL HEALTH 200, LLC.·Product code FMF·November 20, 2023
PENUMBRA CAT6 135CM INDIGO STRAIGHT TIP SYSTEM ASPIRATION CATHETER
FDA Adverse Event
Malfunction
·COVIDIEN·Product code JOL·August 14, 2018
ENDO CLIP II
FDA Adverse Event
Malfunction
·DAVIS & GECK CARIBE LTD·Product code FZP·July 25, 2018
CARDINAL HEALTH
FDA Adverse Event
Malfunction
·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 12, 2024
GOLDVAC SLIM,PUSH BUTTON,10FT
FDA Adverse Event
Malfunction
·BUFFALO FILTER·Product code GEI·June 5, 2019
CARDINALHEALTH
FDA Adverse Event
Malfunction
·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 13, 2024
G1 074735 0083
Certificate
MDD Annex II (excluding section 4)·Covidien llc·TÜV SÜD Product Service GmbH·1 Basic UDI-DI
Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU.
FDA Recall
Terminated
·Nellcor Puritan Bennett Inc. (dba Covidien LP)·Product code CBK·October 1, 2014