← Back to catalogue

Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
NEBULIZER CUP FDA UDI
Model / Reference
HCS4480 FDA UDI
Description
NEBULIZER CUP FDA UDI

Identifiers

Catalog Number
HCS4480 FDA UDI
Primary DI / UDI-DI
00888277692100 FDA UDI
510(k) Number
K091272 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suction/irrigation tubing, single-useTherapeutic agent nebulizer, benchtop

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

Similar devices

Also classified as Therapeutic agent nebulizer, benchtop.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI cc342b27-1c8e-4455-ba6d-f34e39d198fe 36 fields · synced May 29, 2026