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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 5/40 L P DERIVATION FDA UDI
Model / Reference
FV383T FDA UDI
Description
DSV SYSTEM 5/40 L P DERIVATION FDA UDI

Identifiers

Catalog Number
FV383T FDA UDI
Primary DI / UDI-DI
04041906130343 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

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Manufacturer

Manufacturer
Christoph Miethke GmbH & Co. KG

Sources (1)

  • FDA UDI 58f57c62-fc46-4117-86e0-b595db0658d7 36 fields · synced May 30, 2026