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Suction Connection Tube

FDA UDI

Class II (US FDA UDI)

by Shijiazhuang Yuanding Medical Device Co., LTD

Identity

Trade Name
Suction Connection Tube FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
Suction connection tube, Type II, 2200mm FDA UDI
Model / Reference
Type II, 2200mm FDA UDI
Description
Suction connection tube, Type II, 2200mm FDA UDI

Identifiers

Catalog Number
YDSII2200 FDA UDI
Primary DI / UDI-DI
06971092637723 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Suction/irrigation tubing, 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 2200 Millimeter FDA UDI

Category: Suction/irrigation tubing, single-use

Suction Connection Tube by Shijiazhuang Yuanding Medical Device Co., LTD — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5af921d1-7a82-416f-8a4c-ef4923ba98c2 36 fields · synced May 31, 2026