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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Suction/irrigation system canister/bottle holder, single-use FDA UDI
Device Name
DBD-CANISTER,SUCTION,JUMBO JUG,12L,6EA/C FDA UDI
Model / Reference
OR12L FDA UDI
Description
DBD-CANISTER,SUCTION,JUMBO JUG,12L,6EA/C FDA UDI

Identifiers

Catalog Number
OR12L FDA UDI
Primary DI / UDI-DI
10888277634268 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Suction/irrigation system canister/bottle holder, 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

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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suction/irrigation system canister/bottle holder, single-use

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation system canister/bottle holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8aa7805b-ccee-41c1-b96f-17eb5b4f061a 35 fields · synced May 30, 2026