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My Penguin Compressor Nebulizer

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
My Penguin Compressor Nebulizer FDA UDI
Generic Name
Therapeutic agent nebulizer, benchtop FDA UDI
Model / Reference
5608PN FDA UDI

Identifiers

Primary DI / UDI-DI
00840117300026 FDA UDI
510(k) Number
K043238 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Therapeutic agent nebulizer, benchtop

My Penguin Compressor Nebulizer by Dynarex Corp. — 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
Dynarex Corp.

Sources (1)

  • FDA UDI dea6573c-9646-4350-b7e2-eba5159a6302 33 fields · synced May 31, 2026