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Suction Liner

FDA UDI

Class II (US FDA UDI)

by Shijiazhuang Yuanding Medical Device Co., LTD

Identity

Trade Name
Suction Liner FDA UDI
Generic Name
Suction system canister liner FDA UDI
Device Name
YDC suction liner without shutoff filter 2000ml FDA UDI
Model / Reference
YDC suction liner without shutoff filter 2000ml FDA UDI
Description
YDC suction liner without shutoff filter 2000ml FDA UDI

Identifiers

Catalog Number
YDC0020 FDA UDI
Primary DI / UDI-DI
06971092631646 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Suction system canister liner 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

No

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
Total Volume — 2000 Milliliter FDA UDI

Category: Suction system canister liner

Suction Liner 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 system canister liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6d55aa52-5cb4-42ae-8d5b-0871c6bb3b6c 36 fields · synced May 30, 2026