MEIKO MASCHINENBAU GMBH & CO. KG

FDA Device Registration & Listing · OFFENBURG Baden-Wurttemberg, DE · Registration 3006542588

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
3006542588
FEI Number
3006542588
Entity Name
MEIKO MASCHINENBAU GMBH & CO. KG
City/State/Country
OFFENBURG Baden-Wurttemberg, DE
Establishment Address
ENGLERSTRASSE 3, OFFENBURG Baden-Wurttemberg D-77652, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MEIKO Maschinenbau GmbH & Co. KG (Owner Number: 9102540)
Owner / Operator Contact Address
ENGLERSTRASSE 3, --, OFFENBURG, DE-NOTA D-77652, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MEIKO TopLine 10 MEIKO TopLine 20 MEIKO TopLine 40 Type M2 TOPLINE 20 MEIKO:TOPLINE 10 TOPLINE 30 MEIKO TopLine 30 Type M2 TOPLINE 40 MEIKO TopLine 40 MEIKO TopLine 20 Type M2 MEIKO TopLine 10 Type M2 MEIKO TopLine 30

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FLH Washer Of Body Waste Receptacles General Hospital Class 1 880.6800 2007-06-05

Official Correspondent

Ingo Hoffmann

US Agent Details

Dwayne Becknell Business: MEIKO USA Inc. Email: dbecknell@meiko.us Phone: (615) 3996600

Related Public Records

Same Entity

MEIKO Maschinenbau 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 3006542588. Last updated year: 2026. Please use registration number 3006542588 when referencing this establishment in official correspondence.
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