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automatic pressure infusor

FDA UDI

Class I (US FDA UDI)

by Biegler GmbH

Identity

Trade Name
automatic pressure infusor FDA UDI
Generic Name
Intravenous pressure infusor, automated FDA UDI
Device Name
The automatic pressure infusor autopress is used when liquids are to be supplied under constant pressure. FDA UDI
Model / Reference
autopress FDA UDI
Description
The automatic pressure infusor autopress is used when liquids are to be supplied under constant pressure. FDA UDI

Identifiers

Primary DI / UDI-DI
09008247000600 FDA UDI
FDA Product Code
KZD FDA UDI
GMDN Term
Intravenous pressure infusor, automated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5420 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intravenous pressure infusor, automated

automatic pressure infusor by Biegler GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous pressure infusor, automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biegler GmbH

Sources (1)

  • FDA UDI 3a33e059-b786-40dc-b5ba-3c4564a19125 33 fields · synced Jun 8, 2026