HEINZ SCHIEBLER GMBH & CO. KG

FDA Device Registration & Listing · Flensburg Schleswig-Holstein, DE · Registration 8010685

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
8010685
FEI Number
4322
Entity Name
HEINZ SCHIEBLER GMBH & CO. KG
City/State/Country
Flensburg Schleswig-Holstein, DE
Establishment Address
Marienallee 74, Flensburg Schleswig-Holstein 24937, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Heinz Schiebler GmbH & Co. KG (Owner Number: 10042183)
Owner / Operator Contact Address
Marienallee 74, Flensburg, DE-SH 24937, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Easywrap Lymphpad Microfine

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQL Stocking, Medical Support (For General Medical Purposes) General Hospital Class 1 880.5780 2012-10-30

Official Correspondent

Frank Pueschel

US Agent Details

Victor Luciano Business: Haddenham LLC Email: victor.luciano@haddenham.com Phone: (704) 9938677

Related Public Records

Same Entity

Heinz Schiebler 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 8010685. Last updated year: 2026. Please use registration number 8010685 when referencing this establishment in official correspondence.
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