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Atrasorb

FDA UDI

Class I (US FDA UDI)

by Atrasorb Industria De Produtos Hospitalares Ltda

Identity

Trade Name
Atrasorb FDA UDI
Generic Name
Carbon dioxide absorbent FDA UDI
Device Name
Atrasorb Pharma Free - 1 L FDA UDI
Model / Reference
Pharma Free FDA UDI
Description
Atrasorb Pharma Free - 1 L FDA UDI

Identifiers

Catalog Number
9420 FDA UDI
Primary DI / UDI-DI
07898592088956 FDA UDI
FDA Product Code
CBL FDA UDI
GMDN Term
Carbon dioxide absorbent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5300 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Carbon dioxide absorbent

Atrasorb by Atrasorb Industria De Produtos Hospitalares Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbon dioxide absorbent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 45d3fc33-5ac3-4487-8ee1-83f90750e20d 34 fields · synced Jun 8, 2026