← Back to catalogue

ACTion Fuser Pump, 400ml, 1-6 ml/hrDual 190mm caut-to-size catheter

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name
ACTion Fuser Pump, 400ml, 1-6 ml/hrDual 190mm caut-to-size catheter FDA UDI
Generic Name
Elastomeric infusion pump kit FDA UDI
Device Name
ACTion Fuser 400,1-6, Dual 190 Cath Cut, 9"Int,Flow Splitter FDA UDI
Model / Reference
418113400 FDA UDI
Description
ACTion Fuser 400,1-6, Dual 190 Cath Cut, 9"Int,Flow Splitter FDA UDI

Identifiers

Catalog Number
418113400 FDA UDI
Primary DI / UDI-DI
05707480110612 FDA UDI
510(k) Number
K061409 FDA UDI
FDA Product Code
MEB FDA UDI
GMDN Term
Elastomeric infusion pump kit 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

Yes

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

Dimensions & Sizes

Size
Total Volume — 400 Milliliter FDA UDI
Length — 190 Millimeter FDA UDI
Total Volume — 500 Milliliter FDA UDI

Category: Elastomeric infusion pump kit

ACTion Fuser Pump, 400ml, 1-6 ml/hrDual 190mm caut-to-size catheter by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Elastomeric infusion pump kit.

Cleared under the same submission

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
Ambu A/S

Sources (1)

  • FDA UDI 4e4a0ab2-67ca-490d-a329-7950220e0610 38 fields · synced May 30, 2026