CHRISTOPH MIETHKE GMBH & CO.KG

FDA Device Registration & Listing · potsdam Brandenburg, DE · Registration 3015462837

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015462837
FEI Number
3015462837
Entity Name
CHRISTOPH MIETHKE GMBH & CO.KG
City/State/Country
potsdam Brandenburg, DE
Establishment Address
Fritz-von-der-Lancken-Strasse 10, potsdam, potsdam Brandenburg 14469, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
christoph miethke gmbh & co.kg (Owner Number: 10023285)
Owner / Operator Contact Address
ulanenweg 2, potsdam, potsdam, DE-BB 14469, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K192266
PMA Number
N/A

All Registered Proprietary Names

XABO Peritoneal Catheter XABO Ventricular Catheter XABO Catheter Set M.Blue Adjustable Shunt System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GYK Instrument, Shunt System Implantation Neurology Class 1 882.4545 2021-06-09
JXG Shunt, Central Nervous System And Components Neurology Class 2 882.5550 2007-11-15
JXG Shunt, Central Nervous System And Components Neurology Class 2 882.5550 2007-11-15
JXG Shunt, Central Nervous System And Components Neurology Class 2 882.5550 2024-12-20
JXG Shunt, Central Nervous System And Components Neurology Class 2 882.5550 2020-01-08

Official Correspondent

joerg knebel

US Agent Details

Kamaal Anas Business: Aesculap.Inc. Email: kamaal.anas@bbraunusa.com Phone: (610) 9849071

Related Public Records

Same Entity

christoph miethke gmbh & co.kg
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004721439 christoph miethke gmbh & co.kg potsdam Brandenburg, DE

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K981246 Integra Neurocare, LLC BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL850-9730) 1999-05-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015462837. Last updated year: 2026. Please use registration number 3015462837 when referencing this establishment in official correspondence.
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