10,000 results · 26ms · Sources: EU EUDAMED, US FDA

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VCA Lite

FDA UDI
Pce, Inc.·00860009492905·5.3 cc Vaginal Cream Applicator in a 7-pack can...

VCA Lite

FDA UDI
Pce, Inc.·00860009492912·5.3 cc Vaginal Cream Applicator 3-Pack. Three ...

HTI Plastics, a Division of PCE Inc.

Manufacturer
🇺🇸 United States

IDEIA PCE CHLAMYDIA

FDA 510(k)
FDA Class 1 ·Microbiology

VAR (VORTRAN Automatic Resuscitator) with Extension

FDA UDI
VORTRAN MEDICAL TECHNOLOGY 1, INC·10637320050124·The VAR® device is a unique single-patient-use,...

OCI-BL-PCE

Device
EU MDR · Eu Md Class 2a ·CHENGDU OCI MEDICAL DEVICES CO., LTD.·On the market·1 country

HTI Plastics, a Division of PCE Inc.

FDA registration
HTI Plastics, a Division of PCE Inc.·1 product·🇺🇸 United States

PCE Pen Panel Transmitter Box

FDA UDI
NEOCOIL, LLC·00856181003411·The NeoCoil Patient Communication and Entertain...

GLUMA DESENSITIZER SINGLE DOSE 40X1 PCE

FDA UDI
Kulzer GmbH·J014660018540·Agent, tooth bonding resin

GLUMA COMFORT BOND+DESENSIT.SD 40X1 PCE.

FDA UDI
Kulzer GmbH·J014660056640·Agent, tooth bonding resin

GS CUFF2 L (HXA-GCFL-PCE)

Device
EU MDR · Eu Md Class 1 ·OMRON Healthcare Co., Ltd.·On the market·5 countries

GS CUFF2 S (HXA-GCFS-PCE)

Device
EU MDR · Eu Md Class 1 ·OMRON Healthcare Co., Ltd.·On the market·1 country

GS CUFF2 SS (HXA-GCFSS-PCE)

Device
EU MDR · Eu Md Class 1 ·OMRON Healthcare Co., Ltd.·On the market·5 countries

GS CUFF2 XL (HXA-GCFXL-PCE)

Device
EU MDR · Eu Md Class 1 ·OMRON Healthcare Co., Ltd.·On the market·5 countries

GS CUFF2 M (HXA-GCFM-PCE)

Device
EU MDR · Eu Md Class 1 ·OMRON Healthcare Co., Ltd.·On the market·8 countries

PATIENT CONTROLLED EPIDURAL

FDA Adverse Event
Malfunction ·Product code MEA·April 25, 2018

Unique Pull UNIQUE INT Condón 3 PCE

Device
EU MDD · Eu Md Class 2b ·UNIQUE INTERNATIONAL SAS·On the market·32 countries

UNKNOWN

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·April 7, 2022

DAVINCI 5

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 25, 2026

UNKNOWN

FDA Adverse Event
Injury ·MEDTRONIC MEXICO·Product code NDN·July 5, 2022