Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003111059

FEI Number

3003111059

Entity Name

PAUL HARTMANN SAS

City/State/Country

LIEPVRE Haut-Rhin, FR

Establishment Address

ZONE INDUSTRIELLE DE BOIS L'ABBESSE, LIEPVRE Haut-Rhin 68660, FR

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

PAUL HARTMANN AG (Owner Number: 8010690)

Owner / Operator Contact Address

481 Lakeshore Parkway, --, Rock Hill, SC 29730, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dignity Super Multiple Styles Moliform Multiple Styles Dignity, Multiple Styles Dignity Complete Multiple Styles Dignity Extra Multiple Styles Molimed Multiple Styles Dignity Compose Multiple Styles Molicare Multiple Styles

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2007-04-02
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2006-11-15

Official Correspondent

Lee Xiong

US Agent Details

Diane Marsilio Business: HARTMANN USA Email: diane.marsilio@hartmann.info Phone: (803) 9851120

Related Public Records

Same Entity

PAUL HARTMANN AG

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3004623655	PAUL HARTMANN AG	BRUCK Brandenburg, DE
8031008	IVF HARTMANN AG	Neuhausen am Rheinfall Schaffhausen, CH
3029971427	PAUL HARTMANN Manufacturing Sp. z o.o.	Libidza Dolnoslaskie, PL
3003096716	Paul Hartmann Iberia S.A.	Montornes del Valles Barcelona, ES
3002521238	PAUL HARTMANN AG	HERBRECHTINGEN 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 3003111059. Last updated year: 2026. Please use registration number 3003111059 when referencing this establishment in official correspondence.