← Back to catalogue

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 FDA UDI
Device Name
AMAB3000 - AMSORB PLUS JERICAN 5 LITRE FDA UDI
Model / Reference
AMAB3000 FDA UDI
Description
AMAB3000 - AMSORB PLUS JERICAN 5 LITRE FDA UDI

Identifiers

Primary DI / UDI-DI
15059443000001 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

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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Armstrong Medical , Ltd.

Sources (1)

  • FDA UDI d68a5244-d06e-483b-b90a-9e217f4610e5 33 fields · synced Jun 1, 2026