CO2 Source Tubing

FDA UDI

Class II (US FDA UDI)

by Zhejiang Chuangxiang Medical Technology Co., LTD.

Identity

Trade Name: CO2 Source Tubing FDA UDI
Generic Name: Endoscopic insufflation tubing set, single-use FDA UDI
Model / Reference: MD-A-TS-2100 FDA UDI

Identifiers

Primary DI / UDI-DI: 06936534332246 FDA UDI
510(k) Number: K231471 FDA UDI
FDA Product Code: FCX FDA UDI
GMDN Term: Endoscopic insufflation tubing set, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 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

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

CO2 Source Tubing by Zhejiang Chuangxiang Medical Technology Co., LTD. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K231471 also covers:

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: Zhejiang Chuangxiang Medical Technology Co., LTD.

Sources (1)

FDA UDI 57501290-b44c-4362-a5fc-395fb715e8bb 33 fields · synced May 31, 2026