ULRICH GMBH & CO. KG

FDA Device Registration & Listing · Dornstadt Baden-Wurttemberg, DE · Registration 3040111919

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
3040111919
FEI Number
3040111919
Entity Name
ULRICH GMBH & CO. KG
City/State/Country
Dornstadt Baden-Wurttemberg, DE
Establishment Address
Lerchenbergstrasse 15, Dornstadt Baden-Wurttemberg 89160, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ULRICH GMBH & CO. KG (Owner Number: 8010776)
Owner / Operator Contact Address
BUCHBRUNNENWEG 12, --, ULM, DE-BW D-89081, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K252281
PMA Number
N/A

All Registered Proprietary Names

ulrichINJECT CT motion ulricheasyINJECT Max

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IZQ Injector, Contrast Medium, Automatic Cardiovascular Class 2 870.1650 2025-11-25
IZQ Injector, Contrast Medium, Automatic Cardiovascular Class 2 870.1650 2025-11-25

Official Correspondent

No official correspondent registered.

US Agent Details

Eric Gibbs Business: ULRICH MEDICAL USA, INC. Email: regulatory@ulrichmedicalusa.com Phone: (469) 2380832

Related Public Records

Same Entity

ULRICH GMBH & CO. KG
View consolidated registration, premarket clearance, and recall records for this applicant.
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Other Registrations for Same Entity

Registration Number Establishment Name Location
9612420 ULRICH GMBH & CO. KG ULM Baden-Wurttemberg, DE

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040111919. Last updated year: 2026. Please use registration number 3040111919 when referencing this establishment in official correspondence.
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