Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007177447

FEI Number

3007177447

Entity Name

HITTECH MULTIN BV

City/State/Country

Den Haag Zuid-Holland, NL

Establishment Address

Laan van Ypenburg 60, Den Haag Zuid-Holland 2497 GB, NL

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Hittech Multin BV (Owner Number: 10054785)

Owner / Operator Contact Address

Laan van Ypenburg 60, Den Haag, NL-ZH 2497 GB, NL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Cassini

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MMQ	Topographer, Corneal, Ac-Powered	Ophthalmic	Class 1	886.1350	2019-10-25

Official Correspondent

No official correspondent registered.

US Agent Details

Mindy McCann Business: Qserve Group US Inc Email: USagent@qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

Hittech Multin BV

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 3007177447. Last updated year: 2026. Please use registration number 3007177447 when referencing this establishment in official correspondence.