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FDA UDI

Class II (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
drive FDA UDI
Generic Name
Therapeutic agent nebulizer, benchtop FDA UDI
Device Name
Respiratory Conservers Product Description Evolution Conserver,1/ea FDA UDI
Model / Reference
OM-900 FDA UDI
Description
Respiratory Conservers Product Description Evolution Conserver,1/ea FDA UDI

Identifiers

Primary DI / UDI-DI
00822383274485 FDA UDI
510(k) Number
K103392 FDA UDI
FDA Product Code
NFB FDA UDI
GMDN Term
Therapeutic agent nebulizer, benchtop 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Therapeutic agent nebulizer, benchtop

drive by Drive Devilbiss Healthcare — 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

Sources (1)

  • FDA UDI ded8b2d7-b305-40ea-ab3e-c35d956bfc34 34 fields · synced Jun 8, 2026