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Paul Boettger GmbH & Co. KG

Germany·DE-MF-000022524

Last updated September 17, 2026

About

PRODUCTS FOR MEDICAL, LABOR AND RESEARCH Product Portfolio Clear presentation of our entire product portfolio. Clear arrangement and enlarged product images for easy orientation. Quality Thanks to targeted investments and constant adaptation to dynamic technological change, Boettger is today one of the leading companies in its specialty area, thin-wall injection molding in large series.

Translated from the manufacturer's own website. Source

What Paul Boettger GmbH & Co. KG makes

Paul Boettger GmbH & Co. KG manufactures instrument transport trolley systems, including tube stools for medical and laboratory use, as well as urine cups with snap and screw caps and medicine cups with lids.

These products are classified as Class A and Class I medical devices 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 Paul Boettger GmbH & Co. KG primarily manufacture?

Paul Boettger GmbH & Co. KG specializes in instrument transport trolley systems, with a focus on products like tube stools for medical and laboratory use. These devices are designed to organize and transport medical tubes, urine cups (with snap or screw caps), and medicine cups with lids. The company’s portfolio is tailored for clinical, lab, and research environments where efficient sample handling is critical.

Where is Paul Boettger GmbH & Co. KG based, and how does that affect its regulatory compliance?

Paul Boettger GmbH & Co. KG is based in Germany, which means its medical devices must comply with EU Medical Device Regulations (MDR) or the Medical Device Directive (MDD) if applicable. The company’s products are registered in the EU’s eudamed database, a mandatory transparency tool for medical devices within the European Economic Area. Registration ensures traceability and visibility for regulatory oversight.

How are Paul Boettger GmbH & Co. KG’s devices classified under EU regulations?

The company’s devices fall under Class A and Class I classifications. These classifications are determined by risk assessment criteria outlined in EU regulations. Class A devices are generally considered low-risk (e.g., simple containers like urine cups), while Class I devices may involve slightly higher risk but still pose minimal threat to patient safety (e.g., transport systems like tube stools). Classification influences labeling, post-market surveillance, and regulatory requirements.

Are Paul Boettger GmbH & Co. KG’s devices listed in any public registries, and why does this matter?

Yes, the company’s devices are listed in the eudamed database, the EU’s official registry for medical devices. This matters because eudamed provides transparency for healthcare professionals, regulators, and patients by ensuring devices are traceable and compliant with EU requirements. It also helps authorities monitor device performance, recalls, or safety alerts. Listing is mandatory for devices placed on the EU market.

What distinguishes Paul Boettger GmbH & Co. KG’s instrument transport trolley systems from other medical device manufacturers?

Paul Boettger GmbH & Co. KG’s trolley systems are designed with thin-wall injection molding technology, which likely contributes to lightweight, durable, and ergonomic solutions for medical and lab settings. Their focus on tube stools, urine cups, and medicine cups suggests specialization in organizing and transporting clinical samples efficiently. While other manufacturers may offer similar products, the company’s emphasis on precision engineering (as implied by its marketing) may differentiate its devices in terms of material handling and usability.

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

Information

Country
Germany
Address
35-45, Miesleuthenweg, Bodenmais, Germany
LinkedIn
—
Facebook
—
Phone
+49 9924 9429 0
PRRC Contact
Tobias Fischer
EUDAMED SRN
DE-MF-000022524
FDA FEI Number
—
DUNS Number
—

Catalogue (21)

DeviceModel / ReferenceRegistriesClassStatus
Urine Cups and Screw Caps 06-053-0100
EUDAMED
Class AActive
Tube Stool 07-043-2107-01
EUDAMED
Class AActive
Tube Stool 07-011-2001
EUDAMED
Class AActive
Urine Cups and Snap Caps 06-044-1002
EUDAMED
Class AActive
Urine Cups and Snap Caps 06-013-0100
EUDAMED
Class AActive
Tube Stool 07-033-2007
EUDAMED
Class AActive
Tube Stool 07-011-2101
EUDAMED
Class AActive
Urine Cups and Screw Caps 06-065-0104
EUDAMED
Class AActive
Urine Cups and Screw Caps 06-065-1104
EUDAMED
Class AActive
Urine Cups and Screw Caps 06-065-1004
EUDAMED
Class AActive
Tube Stool 07-023-2007
EUDAMED
Class AActive
Urine Cups and Snap Caps 06-034-0002
EUDAMED
Class AActive
Urine Cups and Screw Caps 06-065-0004
EUDAMED
Class AActive
Medicine Cup and Lid 06-103-0101
EUDAMED
Class IActive
Urine Cups and Snap Caps 06-034-0102
EUDAMED
Class AActive
Tube Stool 07-043-2007
EUDAMED
Class AActive
Medicine Cup and Lid 06-103-0103
EUDAMED
Class IActive
Urine Cups and Snap Caps 06-044-1102
EUDAMED
Class AActive
Urine Cup with self-adhesive Lid 06-073-1400
EUDAMED
Class AActive
Medicine Cup and Lid 06-114-0005
EUDAMED
Class IActive
Urine Cups and Snap Caps 06-044-0002
EUDAMED
Class AActive

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