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Drainage Set LiquoGuard 7

FDA UDI

Class II (US FDA UDI)

by Möller Medical GmbH

Identity

Trade Name
Drainage Set LiquoGuard 7 FDA UDI
Generic Name
Cerebrospinal fluid pressure regulation system sensor/tubing set FDA UDI
Device Name
The LiquoGuard 7 tube set consists of a tubing, stop cocks with luer locks, a drainage bag with a reflux valve, adapters to ensure correct insertion into the pump, and a pressure sensor housing with two pressure transducers, a cable for connection to the pump and a sticker to attach the sensor housing to the patient's skin. The tube set is only for use with the LiquoGuard 7. FDA UDI
Model / Reference
00003501 2371 FDA UDI
Description
The LiquoGuard 7 tube set consists of a tubing, stop cocks with luer locks, a drainage bag with a reflux valve, adapters to ensure correct insertion into the pump, and a pressure sensor housing with two pressure transducers, a cable for connection to the pump and a sticker to attach the sensor housing to the patient's skin. The tube set is only for use with the LiquoGuard 7. FDA UDI

Identifiers

Primary DI / UDI-DI
04260277176051 FDA UDI
510(k) Number
K150898 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Cerebrospinal fluid pressure regulation system sensor/tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5550 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

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
MRI Safety
MR Conditional FDA UDI

Category: Cerebrospinal fluid pressure regulation system sensor/tubing set

Drainage Set LiquoGuard 7 by Möller Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cerebrospinal fluid pressure regulation system sensor/tubing set.

Cleared under the same submission

K150898 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Möller Medical GmbH

Sources (1)

  • FDA UDI 08d7a514-d884-4d90-a28b-d3125251a64c 35 fields · synced Jun 9, 2026