HANS FREUDENSTEIN CHIR-MIKROINSTRUMENTE

FDA Device Registration & Listing · PASSAU Bavaria, DE · Registration 8010615

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
8010615
FEI Number
4393
Entity Name
HANS FREUDENSTEIN CHIR-MIKROINSTRUMENTE
City/State/Country
PASSAU Bavaria, DE
Establishment Address
Dr.-Atzinger-Str. 5, PASSAU Bavaria 94036, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
HANS FREUDENSTEIN (Owner Number: 8010615)
Owner / Operator Contact Address
Dr.-Atzinger-Str. 5, --, PASSAU, DE-BY 94036, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HNR Forceps, Ophthalmic Ophthalmic Class 1 886.4350 2001-06-14

Official Correspondent

No official correspondent registered.

US Agent Details

Angelika Scherp Business: BSI - Business Support International Email: info@bsi-fda.com Phone: (212) 3318358

Related Public Records

Same Entity

HANS FREUDENSTEIN
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 8010615. Last updated year: 2026. Please use registration number 8010615 when referencing this establishment in official correspondence.
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