← Back to catalogue

Aesculap

FDA UDI

Class II (US FDA UDI)

by Christoph Miethke GmbH & Co. KG

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Ventriculo-peritoneal/atrial shunt FDA UDI
Device Name
DSV SYSTEM L P DERIVATION 10/30 FDA UDI
Model / Reference
FV163T FDA UDI
Description
DSV SYSTEM L P DERIVATION 10/30 FDA UDI

Identifiers

Catalog Number
FV163T FDA UDI
Primary DI / UDI-DI
04041906107307 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

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
MRI Safety
MR Conditional FDA UDI

Category: Ventriculo-peritoneal/atrial shunt

Aesculap by Christoph Miethke GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventriculo-peritoneal/atrial shunt.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Christoph Miethke GmbH & Co. KG

Sources (1)

  • FDA UDI 0bd4c929-4696-438b-a554-8da08a3dc61b 36 fields · synced May 30, 2026