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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Ultrasonic nebulizing system FDA UDI
Device Name
NEB, KIT, 22 OD OD VALVE T, 6"RES, 7'TUB FDA UDI
Model / Reference
HCS4483VT FDA UDI
Description
NEB, KIT, 22 OD OD VALVE T, 6"RES, 7'TUB FDA UDI

Identifiers

Catalog Number
HCS4483VT FDA UDI
Primary DI / UDI-DI
10888277699229 FDA UDI
510(k) Number
K091272 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Ultrasonic nebulizing system 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

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI
Outer Diameter — 22 Millimeter FDA UDI

Category: Therapeutic agent nebulizer, benchtopUltrasonic nebulizing system

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

Similar devices

Also classified as Ultrasonic nebulizing system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 45a4346e-4611-4229-ad19-b62f108db2a0 37 fields · synced May 30, 2026