1,857 results · 47ms · 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.

PN Medical Inc

Manufacturer
🇺🇸 United States·1 Basic UDI-DI·3 Devices

The Breather Pink

Device
EU MDR · Eu Md Class 1 ·PN Medical Inc·On the market·4 countries

Breather Recover

Device
EU MDR · Eu Md Class 1 ·PN Medical Inc·On the market·4 countries

The Breather

Device
EU MDR · Eu Md Class 1 ·PN Medical Inc·On the market·4 countries

Breather X

FDA UDI
Pn Medical Inc·01240000013849·

The Breather

FDA UDI
Pn Medical Inc·00865202000124·Inspiratory Expiratory Muscle Trainer

The Breather

FDA UDI
Pn Medical Inc·00865202000131·

The Breather

FDA UDI
Pn Medical Inc·08652020001004·Inspiratory Expiratory Muscle Trainer

Breather Voice

FDA UDI
Pn Medical Inc·00850021574116·

Breather Fit

FDA UDI
Pn Medical Inc·00865202000148·

Breather Recover

FDA UDI
Pn Medical Inc·00865202000117·

The Breather Pink

FDA UDI
Pn Medical Inc·00865202000193·

The Breather

Basic UDI-DI
EU MDR · Eu Md Class 1 ·PN Medical Inc·3 devices

CMI

FDA Adverse Event
Other ·COLUMBIA MEDICAL, INC.·Product code HDB·August 13, 1999

9610825-2012-00119

FDA Adverse Event
Malfunction ·Product code FRN·August 15, 2012

CONCERTO, BASIC & SHOWER TROLLEY

FDA Adverse Event
Other ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·March 1, 2011

ID NOW STREP A 2

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code PGX·October 18, 2019

ERBE APC 3

FDA Adverse Event
Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·January 26, 2024

Luft For Life Österreich Ltd

Authorized representative
🇦🇹 Austria·1 Manufacturer·3 Devices

WALLACH PAPETTE KIT

FDA Adverse Event
COOPERSURGICAL INC.·Product code HFE·April 7, 2016