Home GUDID 16932503525234 MT
Primary DI 16932503525234
Brand MT
Company Micro-Tech (Nanjing) Co., Ltd.
Model DILA03002
Device description Dilator Kit(OD=18mm, ID=9.2mm)
Published 2023-08-11
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name KNQ Dilator, Esophageal
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KNQ Dilator, Esophageal Gastroenterology, Urology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 16932503525234 Package GS1 10 In Commercial Distribution 26932503525231 Package GS1 10 In Commercial Distribution 06932503525237 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 16932503525234 16932503525234 26932503525231 26932503525231 06932503525237 06932503525237 6932503525237
GMDN Terms# Term, Definition table Term Definition Endoscopic gastrointestinal stenosis dilator A sterile invasive device intended to be used to dilate or expand a narrowing lesion (e.g., oesophageal stricture, stenosis) in the lumen of the gastrointestinal [GI] tract, under endoscopic visualization. It is made of transparent synthetic polymer material and is available in various forms (e.g., a slender hollow tube through which is passed the endoscope before introduction into the GI tract, or a tapered cap applied to the distal end of the endoscope); the dilator is advanced through the lesion site with direct visualization through the endoscope. This is a single-use device.
Device Sizes# Type, Value, Unit table Type Value Unit Outer Diameter 18 Millimeter
Regulatory Flags# DUNS number 530269083 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex true Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 16932503514658 Biliary Plastic Stent Set BPDS-41114-0712/17 2026-03-20 16932503515617 Biliary Plastic Stent Set BPDS-41114-0715/17 2026-03-20 16932503515624 Biliary Plastic Stent Set BPDS-41114-0718/17 2026-03-20 16932503515631 Biliary Plastic Stent Set BPDS-41114-0805/22 2026-03-20 16932503515648 Biliary Plastic Stent Set BPDS-41114-0807/22 2026-03-20 16932503515655 Biliary Plastic Stent Set BPDS-41114-0809/22 2026-03-20 16932503515662 Biliary Plastic Stent Set BPDS-41114-0812/22 2026-03-20 16932503515679 Biliary Plastic Stent Set BPDS-41114-0815/22 2026-03-20 16932503515686 Biliary Plastic Stent Set BPDS-41114-0818/22 2026-03-20 16932503515693 Biliary Plastic Stent Set BPDS-41114-1005/22 2026-03-20 16932503515709 Biliary Plastic Stent Set BPDS-41114-1007/22 2026-03-20 16932503515716 Biliary Plastic Stent Set BPDS-41114-1009/22 2026-03-20 16932503515723 Biliary Plastic Stent Set BPDS-41114-1012/22 2026-03-20 16932503515730 Biliary Plastic Stent Set BPDS-41114-1015/22 2026-03-20 16932503515747 Biliary Plastic Stent Set BPDS-41114-1018/22 2026-03-20 16932503515754 Biliary Plastic Stent Set BPDS-41114-1105/22 2026-03-20 16932503515761 Biliary Plastic Stent Set BPDS-41114-1107/22 2026-03-20 16932503515778 Biliary Plastic Stent Set BPDS-41114-1109/22 2026-03-20 16932503515785 Biliary Plastic Stent Set BPDS-41114-1112/22 2026-03-20 16932503515792 Biliary Plastic Stent Set BPDS-41114-1115/22 2026-03-20
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