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INTELLAGEN™ Irrigation Pump

FDA UDI

Class III (US FDA UDI)

by Stockert GmbH

Identity

Trade Name
INTELLAGEN™ Irrigation Pump FDA UDI
Generic Name
Bedside infusion pump, single-channel FDA UDI
Device Name
Only commercialized as part of the kit FDA UDI
Model / Reference
20405 FDA UDI
Description
Only commercialized as part of the kit FDA UDI

Identifiers

Catalog Number
M004GEN100204020 FDA UDI
Primary DI / UDI-DI
04260166374117 FDA UDI
FDA Product Code
LPB FDA UDI
OAD FDA UDI
GMDN Term
Bedside infusion pump, single-channel FDA UDI

Classification

Device Class
Class III 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

INTELLAGEN™ Irrigation Pump by Stockert GmbH — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedside infusion pump, single-channel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stockert GmbH

Sources (1)

  • FDA UDI 3f632d1c-c0a4-47fa-b10f-d3ae29d74389 35 fields · synced May 30, 2026