109 results · 73ms · Sources: EU EUDAMED, US FDA

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The Standard. Co., Ltd.

Manufacturer
🇰🇷 South Korea·4 Basic UDI-DIs·4 Devices·4 Importers·SGS Belgium NV and SGS Belgium NV

THE STANDARD CO., LTD.

FDA registration
THE STANDARD CO., LTD.·6 products·🇰🇷 South Korea

Black Eye

FDA UDI
THE STANDARD CO.,LTD.·08809380059002·

Blue Eye

FDA UDI
THE STANDARD CO.,LTD.·08809380050207·

Blue Eye

FDA UDI
THE STANDARD CO.,LTD.·08809380057473·

Blue Eye Submucosal Injection Agent

Device
EU MDD · Eu Md Class 2b ·The Standard. Co., Ltd.·On the market·1 country

ASCENDO submucosal lifting agent

Device
EU MDD · Eu Md Class 2b ·The Standard. Co., Ltd.·On the market·4 countries

Black Eye Endoscopic Marker Ink

Device
EU MDD · Eu Md Class 2b ·The Standard. Co., Ltd.·On the market·1 country

Endoscopic Marker

Device
EU MDD · Eu Md Class 2b ·The Standard. Co., Ltd.·On the market·4 countries

Black Eye Endoscopic Marker Ink

Basic UDI-DI
EU MDD · Eu Md Class 2b ·The Standard. Co., Ltd.·1 device

Blue Eye Submucosal Injection Agent

Basic UDI-DI
EU MDD · Eu Md Class 2b ·The Standard. Co., Ltd.·1 device

ASCENDO Submucosal lifting agent

Basic UDI-DI
EU MDD · Eu Md Class 2b ·The Standard. Co., Ltd.·1 device

Endoscopic Marker

Basic UDI-DI
EU MDD · Eu Md Class 2b ·The Standard. Co., Ltd.·1 device

CMC VASCULAR ACCESS PACK

FDA Adverse Event
Malfunction ·DEROYAL INDUSTRIES, INC.·Product code LRO·July 25, 2023

GC-3PLY-ISO 3 PLY DISPOSABLE MASK

FDA Adverse Event
Malfunction ·NINGBO YIXIN INTELLIGENTIZED SCIENCE AND TECHNOLOGY·Product code LYU·August 20, 2020

FOLEY CATHETER, 2W STD SEC CH16

FDA Adverse Event
Malfunction ·UNOMEDICAL SDN BHD·Product code KOD·January 24, 2013

FOLEY CATHETER, 2W STD SEC CH14

FDA Adverse Event
Malfunction ·UNOMEDICAL SDN BHD·Product code KOD·January 24, 2013

EVIS LUCERA ULTRASOUND GASTROVIDEOSCOPE

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code ODG·June 28, 2021

FOLEY CATHETER, 2W STD SEC CH14

FDA Adverse Event
Malfunction ·UNOMEDICAL SDN BHD·Product code KOD·January 24, 2013

TRACHEAL INTUBATION FIBERSCOPE

FDA Adverse Event
Malfunction ·Product code EOQ·August 2, 2021