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Aero-Pro

FDA UDI

Class II (US FDA UDI)

by Engineered Medical Systems, LLC

Identity

Trade Name
Aero-Pro FDA UDI
Generic Name
Microbial medical gas filter, single-use FDA UDI
Model / Reference
301-439 FDA UDI

Identifiers

Primary DI / UDI-DI
00841470108021 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Microbial medical gas filter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 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: Microbial medical gas filter, single-use

Aero-Pro by Engineered Medical Systems, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microbial medical gas filter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 956206e8-b61d-49eb-b028-4e8a6e0a598d 32 fields · synced May 30, 2026