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Envirotain, LLC

US

Last updated May 24, 2026

What Envirotain, LLC makes

Envirotain, LLC manufactures sharps containers designed for the safe disposal of used needles and other contaminated sharps. These containers are intended for clinical, medical, and home healthcare settings to minimize the risk of needle-stick injuries and ensure proper waste segregation.

The company’s sharps containers are classified as Class II medical devices under U.S. regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The products are developed and distributed from 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 Envirotain, LLC manufacture?

Envirotain, LLC specializes in manufacturing sharps containers. These devices are specifically designed for the safe disposal of used needles and other contaminated sharps, ensuring proper waste segregation and reducing the risk of needle-stick injuries in clinical, medical, and home healthcare settings.

Where is Envirotain, LLC based?

Envirotain, LLC is based in the United States. The company develops and distributes its products from this location.

Which regulatory registries list Envirotain, LLC’s devices?

Envirotain, LLC’s sharps containers are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S.

How are Envirotain, LLC’s devices classified under U.S. regulations?

Envirotain, LLC’s sharps containers fall under the classification of Class II medical devices. This classification is determined based on the level of risk associated with the device, where Class II devices require special controls in addition to general controls to ensure their safety and effectiveness.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
2162555107
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
080390642

Catalogue (36)

DeviceModel / ReferenceRegistriesClassStatus
Mauser WIVA 4 NL050V4080ZWST
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080GEST
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080WIPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080WIGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080ZWST
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080WIPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080GEST
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080ZWGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080ROPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080ZWPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080GEPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080ROPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080ROST
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080ROST
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080ZWGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080ZWPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080WIGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080ROGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080ZWGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080ROGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080WIST
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080ZWST
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080GEST
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080WIGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080GEGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080ROPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080WIST
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080ROST
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080GEGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL060V4080WIST
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080ZWPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080ROGR
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080GEPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL030V4080GEPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080WIPO
FDA UDI
Class IIActive
Mauser WIVA 4 NL050V4080GEGR
FDA UDI
Class IIActive

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