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Dual Port Device with two integral silicone valves

FDA UDI

Class II (US FDA UDI)

by Hummingbird Med Devices Inc

Identity

Trade Name
Dual Port Device with two integral silicone valves FDA UDI
Generic Name
Intravenous line stopcock FDA UDI
Device Name
Dual Port Device with two integral silicone valves a component for the blood draw system FDA UDI
Model / Reference
DPD-HM-2 FDA UDI
Description
Dual Port Device with two integral silicone valves a component for the blood draw system FDA UDI

Identifiers

Primary DI / UDI-DI
00850584007021 FDA UDI
FDA Product Code
FMG FDA UDI
GMDN Term
Intravenous line stopcock FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intravenous line stopcock

Dual Port Device with two integral silicone valves by Hummingbird Med Devices Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous line stopcock.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a033b03d-4f68-440b-8167-e9c36ecb55e5 34 fields · synced May 30, 2026