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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Enteral feeding/decompression tube clearing stem FDA UDI
Device Name
QCW CLOG REMOVER,ORANGE 18FR-24FRX21.5CM FDA UDI
Model / Reference
ENT922 FDA UDI
Description
QCW CLOG REMOVER,ORANGE 18FR-24FRX21.5CM FDA UDI

Identifiers

Catalog Number
ENT922 FDA UDI
Primary DI / UDI-DI
10888277699830 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Enteral feeding/decompression tube clearing stem FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

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

Dimensions & Sizes

Size
Length — 21.5 Centimeter FDA UDI

Category: Enteral feeding/decompression tube clearing stem

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

Similar devices

Also classified as Enteral feeding/decompression tube clearing stem.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 63b2f15e-9f37-475e-a123-8306a03f6d8c 37 fields · synced Jun 6, 2026