Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003920322

FEI Number

3003920322

Entity Name

VACUTEC MESSTECHNIK GMBH

City/State/Country

DRESDEN Saxony, DE

Establishment Address

DORNBLUTHSTR.14a, DRESDEN Saxony D-01277, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

VacuTec Messtechnik (Owner Number: 9026010)

Owner / Operator Contact Address

Dornbluthstr. 14a, --, Dresden, DE-NOTA D-01277, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VacuDAP-C Bluetooth® duo VacuDAP fluoro VacuDAP Bluetooth® duo VacuDAP-Bluetooth® VacuDAP compact VacuDAP-OEM VacuDAP standard VacuDAP-C VacuDAP duo VacuDAP OEM duo VacuDAP twin VacuDAP-C duo VacuDAP 2004 OEM AEC sensor

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LHO	Instrument, Quality-Assurance, Radiologic	Radiology	Class 1	892.1940	2003-06-16

Official Correspondent

Dong Thuc Knobbe

US Agent Details

Jennifer Dolan Business: RTI Group North America Email: jennifer.dolan@rtigroup.com Phone: (973) 4390242

Related Public Records

Same Entity

VacuTec Messtechnik

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 3003920322. Last updated year: 2026. Please use registration number 3003920322 when referencing this establishment in official correspondence.