Suction Tube

FDA UDI

Class II (US FDA UDI)

by Yangzhou Fartley Medical Instrument Technology Co., Ltd.

Identity

Trade Name: Suction Tube FDA UDI
Generic Name: Endoscopic insufflation tubing set, single-use FDA UDI
Device Name: Sentrus Suction Tubing, Suction Tubing, 3/16" FDA UDI
Model / Reference: FTL-ST-316-360 FDA UDI
Description: Sentrus Suction Tubing, Suction Tubing, 3/16" FDA UDI

Identifiers

Catalog Number: SEN-ST-316-360 FDA UDI
Primary DI / UDI-DI: 06936603231043 FDA UDI
FDA Product Code: BYY FDA UDI
GMDN Term: Endoscopic insufflation tubing set, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6740 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Endoscopic insufflation tubing set, single-use

Suction Tube by Yangzhou Fartley Medical Instrument Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Endoscopic insufflation tubing set, single-use.

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Insufflation Tubing, Universal — Northgate Technologies Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Yangzhou Fartley Medical Instrument Technology Co., Ltd.

Sources (1)

FDA UDI 2fc5f90a-acf2-4a86-ac73-8145e73ff34f 34 fields · synced Jun 1, 2026