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VORTRAN PercussiveNEB 2.0

FDA UDI

Class II (US FDA UDI)

by Vortran Medical Technology 1, Inc.

Identity

Trade Name
VORTRAN PercussiveNEB 2.0 FDA UDI
Generic Name
Ultrasonic nebulizing system FDA UDI
Device Name
The PercussiveNEB 2.0 is an intrapulmonary percussive treatment device that incorporates a nebulizer which delivers aerosolized medication and is designed to oscillate during exhalation and inhalation to help remove endobronchial secretions. FDA UDI
Model / Reference
8030 FDA UDI
Description
The PercussiveNEB 2.0 is an intrapulmonary percussive treatment device that incorporates a nebulizer which delivers aerosolized medication and is designed to oscillate during exhalation and inhalation to help remove endobronchial secretions. FDA UDI

Identifiers

Catalog Number
8030 FDA UDI
Primary DI / UDI-DI
10637320080305 FDA UDI
510(k) Number
K003684 FDA UDI
FDA Product Code
NHJ FDA UDI
GMDN Term
Ultrasonic nebulizing system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

Category: Ultrasonic nebulizing system

VORTRAN PercussiveNEB 2.0 by Vortran Medical Technology 1, 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 a3a93cda-f594-4dc5-b0a5-22b690c721d2 36 fields · synced Jun 8, 2026