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True Integral

FDA UDI

Class II (US FDA UDI)

by True Integral Inc

Identity

Trade Name
True Integral FDA UDI
Generic Name
Therapeutic agent nebulizer, benchtop FDA UDI
Device Name
Intelligent Mesh Nebulizer FDA UDI
Model / Reference
NEB002 FDA UDI
Description
Intelligent Mesh Nebulizer FDA UDI

Identifiers

Primary DI / UDI-DI
00860003079706 FDA UDI
510(k) Number
K171549 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Therapeutic agent nebulizer, benchtop 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Therapeutic agent nebulizer, benchtop

True Integral by True Integral 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

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Manufacturer

Manufacturer
True Integral Inc

Sources (1)

  • FDA UDI ce7ab922-15aa-49b6-8bd8-75367849278d 34 fields · synced May 29, 2026