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Dispenser DP 30 LipoPlus

FDA UDI

Class II (US FDA UDI)

by Nouvag AG

Identity

Trade Name
Dispenser DP 30 LipoPlus FDA UDI
Generic Name
Bedside infusion pump, single-channel FDA UDI
Device Name
Infiltration pump FDA UDI
Model / Reference
4181US FDA UDI
Description
Infiltration pump FDA UDI

Identifiers

Primary DI / UDI-DI
ENOU4181US0 FDA UDI
510(k) Number
K071588 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Bedside infusion pump, single-channel 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bedside infusion pump, single-channel

Dispenser DP 30 LipoPlus by Nouvag AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedside infusion pump, single-channel.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nouvag AG

Sources (1)

  • FDA UDI 48728bcc-8d32-459d-ae1f-a5213089122b 35 fields · synced Jun 8, 2026