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Aria

FDA UDI

Class I (US FDA UDI)

by Molecular Products Inc

Identity

Trade Name
Aria FDA UDI
Generic Name
Carbon dioxide absorber, single-use FDA UDI
Device Name
CO2 Assembly, Sodasorb HMED, W-V Indicating, Aria FDA UDI
Model / Reference
PC02-0005 FDA UDI
Description
CO2 Assembly, Sodasorb HMED, W-V Indicating, Aria FDA UDI

Identifiers

Primary DI / UDI-DI
00850039679124 FDA UDI
FDA Product Code
BSF FDA UDI
GMDN Term
Carbon dioxide absorber, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5310 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Carbon dioxide absorber, single-use

Aria by Molecular Products Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbon dioxide absorber, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f686f0b6-fc2a-40d3-a5ae-397f79d99fb1 35 fields · synced May 30, 2026