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ACTion Fuser Pump, 200ml, 5-15 ml/hr, 140mm caut-to-size catheter

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name
ACTion Fuser Pump, 200ml, 5-15 ml/hr,140mm caut-to-size catheter FDA UDI
Generic Name
Elastomeric infusion pump kit FDA UDI
Device Name
ACTion Fuser 200,5-15ml/hr,140mm Cut-to-size, prosit,6" intr FDA UDI
Model / Reference
418117200 FDA UDI
Description
ACTion Fuser 200,5-15ml/hr,140mm Cut-to-size, prosit,6" intr FDA UDI

Identifiers

Catalog Number
418117200 FDA UDI
Primary DI / UDI-DI
05707480121533 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
Length — 140 Millimeter FDA UDI
Total Volume — 300 Milliliter FDA UDI
Total Volume — 200 Milliliter FDA UDI

Category: Elastomeric infusion pump kit

ACTion Fuser Pump, 200ml, 5-15 ml/hr, 140mm 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

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Manufacturer

Manufacturer
Ambu A/S

Sources (1)

  • FDA UDI 64fd4da8-c1db-4ec0-a7c6-2de96670efb6 38 fields · synced May 30, 2026