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Pocket Air

FDA UDIEUDAMED

Class II (US FDA UDI)

by Microbase Technology Corp.

Identity

Trade Name
POCKET AIR FDA UDI
Generic Name
Therapeutic agent nebulizer, benchtop FDA UDI
Model / Reference
MBPN002 FDA UDI

Identifiers

Primary DI / UDI-DI
04719874690069 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Therapeutic agent nebulizer, benchtop

Pocket Air by Microbase Technology Corp. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Therapeutic agent nebulizer, benchtop.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 7d346669-e679-43f6-bb1b-ef8e4bf3cf04 32 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026