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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
Cerebrospinal fluid shunt connector FDA UDI
Device Name
CONNECTOR L-SHAPE FDA UDI
Model / Reference
FV051T FDA UDI
Description
CONNECTOR L-SHAPE FDA UDI

Identifiers

Catalog Number
FV051T FDA UDI
Primary DI / UDI-DI
04041906130022 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Cerebrospinal fluid shunt connector 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

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 shunt connector

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

Similar devices

Also classified as Cerebrospinal fluid shunt connector.

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 419a60a2-e977-4205-a1f8-d1f16070fefc 35 fields · synced Jun 8, 2026