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Ambu® ACTion™ Fuser Pump

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name
Ambu® ACTion™ Fuser Pump FDA UDI
Generic Name
Mechanical infusion pump administration set FDA UDI
Device Name
Action Fuser, 650 mL, 5-15 mL/hr Reg, 140 mm Cath, 6" Intro FDA UDI
Model / Reference
418104650M FDA UDI
Description
Action Fuser, 650 mL, 5-15 mL/hr Reg, 140 mm Cath, 6" Intro FDA UDI

Identifiers

Catalog Number
418104650M FDA UDI
Primary DI / UDI-DI
05707480156108 FDA UDI
510(k) Number
K061409 FDA UDI
FDA Product Code
MEB FDA UDI
GMDN Term
Mechanical infusion pump administration set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Total Volume — 650 Milliliter FDA UDI

Category: Mechanical infusion pump administration set

Ambu® ACTion™ Fuser Pump by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mechanical infusion pump administration set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ambu A/S

Sources (1)

  • FDA UDI 3b831c05-b48b-4a4b-b140-ac6332772e77 38 fields · synced Jun 8, 2026