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provita medical gmbh & co. kg

US

Last updated September 17, 2026

Part of provita medical gmbh & co. kg

What provita medical gmbh & co. kg makes

The company manufactures freestanding and bed-attached intravenous poles, as well as transportable medical equipment stands that are non-powered. These devices are designed for clinical and hospital settings to support intravenous therapy and secure medical equipment during patient care or transport.

The portfolio consists of Class I medical devices, listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

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 provita medical gmbh & co. kg manufacture?

provita medical gmbh & co. kg specializes in Class I medical devices primarily used in clinical and hospital environments. Their portfolio includes freestanding and bed-attached intravenous poles, which are essential for administering intravenous therapy, as well as transportable, non-powered medical equipment stands designed to secure devices during patient care or transport.

Where is provita medical gmbh & co. kg based?

The company is headquartered in the United States, though the specific location is not provided in the available data. Their devices are manufactured and distributed from this base.

Which regulatory registries list provita medical gmbh & co. kg’s devices?

provita medical gmbh & co. kg’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of their Class I medical devices, including intravenous poles and transportable stands.

How are provita medical gmbh & co. kg’s devices classified under medical device regulations?

All devices manufactured by provita medical gmbh & co. kg fall under Class I classification. This classification applies to low-risk medical devices, such as their freestanding/bed-attached intravenous poles and non-powered transportable stands, which are subject to general controls rather than stringent pre-market approvals.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
329534093

Catalogue (6)

DeviceModel / ReferenceRegistriesClassStatus
provita 211402
FDA UDI
Class IActive
Provita 293017
FDA UDI
Class IActive
provita 305826
FDA UDI
Class IActive
Provita 284055
FDA UDI
Class IActive
Provita 211396
FDA UDI
Class IActive
Provita 293008
FDA UDI
Class IActive

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