Eckart KLOBE

FDA Device Registration & Listing · Mannheim Baden-Wurttemberg, DE · Registration 3009562727

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
3009562727
FEI Number
3009562727
Entity Name
Eckart KLOBE
City/State/Country
Mannheim Baden-Wurttemberg, DE
Establishment Address
M 7, 9a-10, Mannheim Baden-Wurttemberg 68161, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Klobe (Owner Number: 10040380)
Owner / Operator Contact Address
M 7, 9a-10, Mannheim, DE-BW 68161, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Eckart Klobe Vacuum Bell

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IPT Orthosis, Thoracic Physical Medicine Class 1 890.3490 2012-04-06

Official Correspondent

Eckart Klobe

US Agent Details

Stefanie D. Bankston Email: vigilance@beoberlin.eu Phone: (713) 4834617

Related Public Records

Same Entity

Klobe
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009562727. Last updated year: 2026. Please use registration number 3009562727 when referencing this establishment in official correspondence.
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