Skip to content

Medela AG

Switzerland CH-MF-000018913 Last updated 25 Oct 2026

Devices
197
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue197

Page 1 of 4

Showing 1-50 of 197

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

TÜV SÜD Product Service GmbH 0123 1 certificate

  • G10 011634 0235 Supplemented Expires in 83 days

    Quality management system EU MDR

    Issued
    27 Aug 2026
    Expires
    16 Jan 2027
    Reason
    Add device or group

Notified bodies

About

Medela aims to promote the health of you and your baby thanks to the benefits of breast milk. We provide you with solutions and information about breastfeeding

From the manufacturer's own website. Source

What Medela AG makes

Medela AG manufactures sterile breast pump accessories, including the Thopaz and Thopaz+ systems, along with single-use feeding bottles designed for infant nutrition.

These devices are classified as Class I and Class IIa under EU regulations and are listed in the EUDAMED registry. The company is based in Switzerland.

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 Medela AG manufacture?

Medela AG specializes in devices related to breastfeeding and infant nutrition. Specifically, they produce sterile breast pump accessories, such as the Thopaz and Thopaz+ systems, as well as single-use feeding bottles. These products are designed to support breastfeeding and ensure safe feeding for infants.

Where is Medela AG based?

Medela AG is headquartered in Switzerland. The company’s Swiss location reflects its commitment to manufacturing and distributing medical devices that meet international standards for safety and quality.

In which regulatory registries are Medela AG’s devices listed?

Medela AG’s devices are listed in the EUDAMED registry, which is the European Union’s database for medical devices. This registry helps ensure transparency and traceability of devices authorized for use within the EU market.

How are Medela AG’s devices classified under EU regulations?

Medela AG’s devices fall under Class I and Class IIa classifications according to EU medical device regulations. Class I devices are generally low-risk, while Class IIa devices pose a slightly higher risk and require additional safety measures, such as design controls and risk management.

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

Information

Country
Switzerland
Address
4b, Lättichstrasse, Baar, Switzerland
Phone
+1-877-735-1626
EUDAMED SRN
CH-MF-000018913
FDA FEI number
3002807523
DUNS number
488293218