ECKERT & ZIEGLER BEBIG GMBH

FDA Device Registration & Listing · BERLIN, DE · Registration 9617477

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
9617477
FEI Number
1000310011
Entity Name
ECKERT & ZIEGLER BEBIG GMBH
City/State/Country
BERLIN, DE
Establishment Address
ROBERT-ROSSLE STR.10, BERLIN 13125, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ECKERT & ZIEGLER BEBIG GmbH (Owner Number: 9034266)
Owner / Operator Contact Address
ROBERT-ROSSLE STR.10, --, BERLIN, DE-BE 13125, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K931393
PMA Number
N/A

All Registered Proprietary Names

Ru-106 Eye Applicators

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KXK Source, Brachytherapy, Radionuclide Radiology Class 2 892.5730 2011-02-10

Official Correspondent

No official correspondent registered.

US Agent Details

Ana R. Ramirez Business: Eckert & Ziegler Isotope Products Email: ana.ramirez@ezag.com Phone: (661) 3091034

Related Public Records

Same Entity

ECKERT & ZIEGLER BEBIG GmbH
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 9617477. Last updated year: 2026. Please use registration number 9617477 when referencing this establishment in official correspondence.
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