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Amsorb® Plus

FDA UDI

Class I (US FDA UDI)

by Armstrong Medical , Ltd.

Identity

Trade Name
AMSORB® PLUS FDA UDI
Generic Name
Carbon dioxide absorbent cartridge FDA UDI
Device Name
AMAB3801GE 2105489-003 AMSORB PLUS PREFILLED G-CAN 1.0L FDA UDI
Model / Reference
AMAB3801GE FDA UDI
Description
AMAB3801GE 2105489-003 AMSORB PLUS PREFILLED G-CAN 1.0L FDA UDI

Identifiers

Primary DI / UDI-DI
05060505643701 FDA UDI
FDA Product Code
CBL FDA UDI
GMDN Term
Carbon dioxide absorbent cartridge 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 cartridge

Amsorb® Plus by Armstrong Medical , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbon dioxide absorbent cartridge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Armstrong Medical , Ltd.

Sources (1)

  • FDA UDI b3c02938-a358-4c4f-bc8b-110c1d860fec 33 fields · synced Jun 1, 2026