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Procedure Products waste bags

FDA UDI

Class II (US FDA UDI)

by Procedure Products, Inc.

Identity

Trade Name
Procedure Products waste bags FDA UDI
Generic Name
Extracorporeal circuit waste bag FDA UDI
Device Name
Waste bag with dual check valve FDA UDI
Model / Reference
4559 FDA UDI
Description
Waste bag with dual check valve FDA UDI

Identifiers

Primary DI / UDI-DI
B16045591 FDA UDI
510(k) Number
K874037 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Extracorporeal circuit waste bag FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Extracorporeal circuit waste bag

Procedure Products waste bags by Procedure Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extracorporeal circuit waste bag.

Cleared under the same submission

K874037 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Procedure Products, Inc.

Sources (1)

  • FDA UDI c3a8d29e-c57f-4e4a-8938-dc810c1095a9 34 fields · synced Jun 8, 2026