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Du-O-Vac Canister

FDA UDI

Class II (US FDA UDI)

by W.t. Farley, Inc.

Identity

Trade Name
Du-O-Vac Canister FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
Collection Canister for Du-O-Vac, 10 Pack FDA UDI
Model / Reference
DV-3-110 FDA UDI
Description
Collection Canister for Du-O-Vac, 10 Pack FDA UDI

Identifiers

Primary DI / UDI-DI
10856438007916 FDA UDI
510(k) Number
K781988 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Surgical suction system collection container, 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Surgical suction system collection container, single-use

Du-O-Vac Canister by W.t. Farley, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W.t. Farley, Inc.

Sources (1)

  • FDA UDI 16b62287-def7-43f0-ab1e-b50c9b372186 35 fields · synced May 30, 2026