SCHUCHMANN GMBH & CO. KG

FDA Device Registration & Listing · Bissendorf Lower Saxony, DE · Registration 3017004793

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
3017004793
FEI Number
3017004793
Entity Name
SCHUCHMANN GMBH & CO. KG
City/State/Country
Bissendorf Lower Saxony, DE
Establishment Address
Rudolf-Runge-Strasse 3, Bissendorf Lower Saxony 49143, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Schuchmann Gmbh & Co. KG (Owner Number: 10081851)
Owner / Operator Contact Address
Rudolf-Runge-Strasse 3, Bissendorf, DE-NI 49143, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Schuchmann

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITJ Walker, Mechanical Physical Medicine Class 1 890.3825 2021-05-20

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Schuchmann Gmbh & Co. KG
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017004793. Last updated year: 2026. Please use registration number 3017004793 when referencing this establishment in official correspondence.
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