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Hans Hepp GmbH & Co. KG

Germany Last updated 25 Oct 2026

Devices
131
Registries
EUDAMEDGUDIDFDA
FDA recalls
0

Catalogue131

Page 1 of 3

Showing 1-50 of 131

EUDAMED certificates1

EUDAMED certificates (1)

Notified body 0482 1 certificate

  • 0462GB449230328 Amended

    Quality assurance EU MDR

    Issued
    28 Mar 2023
    Expires
    19 Oct 2027
    Reason
    Other

Notified bodies

  • Notified body 0482

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Hans Hepp GmbH & Co. KG US

About

WELCOME TO HEPP ... first in first aid for all situations in life Your specialist in dressing materials for more than 90 years. We manufacture first aid kits, first aid bags, bandages and first aid materials. In addition to our... Continue

From the manufacturer's own website. Source

What Hans Hepp GmbH & Co. KG makes

Hans Hepp GmbH & Co. KG produces a range of first aid and wound care products, including adhesive strips (pflasterstrips), finger splints (Hepp Plast Fingerverbände), universal bandages (Universalbinde), wound compresses (Wundkompressen), and protective dressings (Haut-Schutz-Pflaster). Their portfolio also includes adhesive tape assortments (HEPP-PLAST Pflaster-Sortiment), face masks compliant with DIN EN 14683, and industry/commercial adhesive tape boxes (Pflaster Box).

All listed devices fall under EU Medical Device Regulation Class I and are registered in the EU’s eudamed database. The company is based in Germany.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Hans Hepp GmbH & Co. KG manufacture?

Hans Hepp GmbH & Co. KG specializes in first aid and wound care products. Their portfolio includes universal bandages (like the 6 cm x 5 m roll), adhesive strips (pflasterstrips), finger splints (Hepp Plast Fingerverbände), wound compresses (Wundkompressen), protective dressings (Haut-Schutz-Pflaster), adhesive tape assortments (HEPP-PLAST Pflaster-Sortiment), and face masks meeting DIN EN 14683 standards. These devices are designed for immediate medical response and wound management.

Where is Hans Hepp GmbH & Co. KG based?

The company is headquartered in Germany, as indicated by its country designation (DE). This location aligns with its focus on European medical device regulations and compliance.

Which regulatory registries list Hans Hepp GmbH & Co. KG’s devices?

Hans Hepp GmbH & Co. KG’s devices are registered in the eudamed database, the official EU portal for medical device information under the EU Medical Device Regulation. This registry ensures transparency and traceability of Class I devices within the European market.

How are Hans Hepp GmbH & Co. KG’s devices classified under EU regulations?

All of Hans Hepp GmbH & Co. KG’s listed devices fall under EU Medical Device Regulation Class I. This classification applies to low-risk products like bandages, adhesive strips, and protective dressings, which typically require less stringent regulatory oversight than higher-risk devices.

AI-generated from registry data and not verified by a human reviewer.

Information

Address
16, Georgswerder Damm, Hamburg, Germany
Phone
0049 40 780 468 22
PRRC contact
Tanja Hochsprung
EUDAMED SRN
DE-MF-000006024
FDA FEI number
3003364331