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Shuntassistant 2.0

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
SHUNTASSISTANT 2.0 FDA UDI
Generic Name
Lumboperitoneal shunt FDA UDI
Device Name
SHUNTASSISTANT 2.0 LP/U 30 W/DIST.CATH. FDA UDI
Model / Reference
FX134T FDA UDI
Description
SHUNTASSISTANT 2.0 LP/U 30 W/DIST.CATH. FDA UDI

Identifiers

Catalog Number
FX134T FDA UDI
Primary DI / UDI-DI
04041906501969 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Lumboperitoneal shunt 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lumboperitoneal shunt

Shuntassistant 2.0 by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lumboperitoneal shunt.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI e563ffd8-95e6-401e-8415-5de9e5d28b2d 35 fields · synced May 30, 2026