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Imtegra GmbH & Co KG

Germany·DE-MF-000006451

Last updated September 17, 2026

About

OP sets, cover towels, suction cups, suction hoses, suction bag and medical consumables for surgically active doctors, medical care centers and clinics

From the manufacturer's own website. Source

What Imtegra GmbH & Co KG makes

Imtegra provides single-use, non-medicated ophthalmic surgical procedure kits designed for surgical procedures. These kits include essential components such as OP sets, cover towels, suction cups, suction hoses, and suction bags tailored for use in medical care centers and clinics.

The company’s products fall under EU device classes Class I and Class IIa, and they are registered in the EU’s eudamed database. Imtegra GmbH & Co KG 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 Imtegra GmbH & Co KG manufacture?

Imtegra GmbH & Co KG specializes in single-use, non-medicated ophthalmic surgical procedure kits. These kits include essential components like OP sets, cover towels, suction cups, suction hoses, and suction bags. The company’s focus is on providing consumables and tools designed specifically for surgical procedures in medical care centers and clinics.

Where is Imtegra GmbH & Co KG based?

Imtegra GmbH & Co KG is based in Germany. The company’s location in Germany aligns with its role as a European manufacturer supplying medical devices to healthcare providers across the region.

Which regulatory registries list Imtegra’s devices?

Imtegra’s devices are listed in the EU’s eudamed database, which serves as the official registry for medical devices within the European Union. This registration ensures transparency and compliance with EU medical device regulations.

How are Imtegra’s devices classified under EU regulations?

Imtegra’s devices fall under EU device classes Class I and Class IIa. The classification is determined by factors like the intended use, duration of contact with the body, and potential risks. Class I devices are generally low-risk, while Class IIa devices pose a slightly higher risk and require additional scrutiny to ensure safety and performance.

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

Information

Country
Germany
Address
15, Industriestrasse, Rostock, Germany
LinkedIn
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Facebook
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Phone
+493811217210
PRRC Contact
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EUDAMED SRN
DE-MF-000006451
FDA FEI Number
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DUNS Number
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Catalogue (399)

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