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FARMABAN SA

US

Last updated May 30, 2026

What FARMABAN SA makes

Farmaban SA manufactures adhesive bandages designed for wound care and minor skin protection. Their product line includes hypoallergenic and breathable tape formulations intended for medical and first-aid applications, such as securing dressings or covering small injuries.

The company’s adhesive bandages fall under FDA Class I medical devices and are listed in the FDA’s Unique Device Identification (UDI) system. The portfolio is regulated under the US Food and Drug Administration’s compliance framework, with devices subject to general controls and registration requirements.

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 Farmaban SA manufacture?

Farmaban SA specializes in adhesive bandages primarily used for wound care and minor skin protection. Their products are designed for medical and first-aid applications, such as securing dressings or covering small injuries. The company focuses on hypoallergenic and breathable tape formulations to ensure compatibility with sensitive skin.

Where is Farmaban SA based, and how does that affect its regulatory compliance?

Farmaban SA is based in the United States, which means its devices are regulated under the US Food and Drug Administration (FDA). Since their adhesive bandages fall under FDA Class I classification, they are subject to general controls and registration requirements, including listing in the FDA’s Unique Device Identification (UDI) system.

Which regulatory registries or databases list Farmaban SA’s devices?

Farmaban SA’s adhesive bandages are included in the FDA’s Unique Device Identification (UDI) system. This database helps track and verify the identity of medical devices in the US market, ensuring traceability and compliance with regulatory standards.

How are Farmaban SA’s adhesive bandages classified by regulatory authorities?

Farmaban SA’s adhesive bandages are classified as FDA Class I medical devices. This classification is typically assigned to low-risk devices that pose minimal potential harm to users, meaning they are subject to general controls rather than strict pre-market approval processes.

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

Information

Country
US
Address
—
Website
farmaban.com
LinkedIn
—
Facebook
—
Phone
+34938789507
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
470774852

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
AC-tape Plus 64210000
FDA UDI
Class IActive
AC-tape Plus 64310000
FDA UDI
Class IActive
AC-tape Plus 64410000
FDA UDI
Class IActive
AC-tape Plus 65310000
FDA UDI
Class IActive
AC-tape Plus 65210000
FDA UDI
Class IActive

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