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Yukon Medical, LLC

United States·US-MF-000027131

Last updated September 17, 2026

What Yukon Medical, LLC makes

Yukon Medical, LLC manufactures vial/bottle adaptors (both hermetic and non-hermetic), negative-pressure intravenous line needleless valve-connectors, and non-ISO80369 formatted bag access spikes. Their product portfolio includes devices such as ViaLok, SmartSite, and Arisure.

The company's devices are regulated as Class I, Class II, and Class IIa medical devices and are listed in eudamed, fda_510k, and fda_udi registries. Yukon Medical, LLC is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does Yukon Medical, LLC manufacture?

Yukon Medical, LLC manufactures vial/bottle adaptors (both hermetic and non-hermetic), negative-pressure intravenous line needleless valve-connectors, and non-ISO80369 formatted bag access spikes. Their product portfolio includes devices such as ViaLok, SmartSite, and Arisure.

Where is Yukon Medical, LLC based?

Yukon Medical, LLC is based in the United States. The company operates from its headquarters located in the US, where it designs and manufactures its medical devices.

Which regulatory registries list Yukon Medical's devices?

Yukon Medical's devices are listed in several regulatory registries including eudamed, fda_510k, and fda_udi. These registries track medical devices for regulatory purposes and market surveillance.

How are Yukon Medical's devices classified?

Yukon Medical's devices are regulated as Class I, Class II, and Class IIa medical devices. The classification depends on the specific device and its associated level of risk, with Class I being the lowest risk and Class IIa being moderate risk.

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

Information

Country
United States
Address
4021 Stirrup Creek Drive , Durham, United States
LinkedIn
—
Facebook
—
Phone
9195958250
PRRC Contact
Pamela McNulty
EUDAMED SRN
US-MF-000027131
FDA FEI Number
3009631669
DUNS Number
963361170

Catalogue (57)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Arisure YM054
EUDAMEDFDA UDI
Class IIaActive
Arisure YM053
EUDAMEDFDA UDI
Class IIaActive
Arisure YM060
EUDAMEDFDA UDI
Class IIaActive
BD SmartSite MV0413-0006
EUDAMED
Class IActive
ViaLok YM038
EUDAMEDFDA UDI
Class IActive
ViaLok YM033
EUDAMEDFDA UDI
Class IActive
Arisure YM051
EUDAMEDFDA UDI
Class IIaActive

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