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Xabo

FDA UDI

Class II (US FDA UDI)

by Christoph Miethke GmbH & Co. KG

Identity

Trade Name
XABO FDA UDI
Generic Name
Ventriculo-peritoneal/atrial shunt FDA UDI
Device Name
XABO CATHETER SET W/VENTR.CATHETER 180MM FDA UDI
Model / Reference
FY040A FDA UDI
Description
XABO CATHETER SET W/VENTR.CATHETER 180MM FDA UDI

Identifiers

Catalog Number
FY040A FDA UDI
Primary DI / UDI-DI
04041906506742 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Ventriculo-peritoneal/atrial 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

Yes

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 Safe FDA UDI

Category: Ventriculo-peritoneal/atrial shunt

A comprehensive medical device directory listing the XABO ventricle-peritoneal/atrial shunt, a treatment for increased intracranial pressure.

Similar devices

Also classified as Ventriculo-peritoneal/atrial shunt.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Christoph Miethke GmbH & Co. KG

Sources (1)

  • FDA UDI 724e24e9-22f9-406b-95f3-921f31fa6a13 36 fields · synced Jul 9, 2026