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Manifold

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Manifold FDA UDI
Generic Name
Fluid transfer set, general-purpose FDA UDI
Device Name
2 Port Manifold - Right/Off/Block Body - 500 PSI FDA UDI
Model / Reference
193111 FDA UDI
Description
2 Port Manifold - Right/Off/Block Body - 500 PSI FDA UDI

Identifiers

Catalog Number
193111 FDA UDI
Primary DI / UDI-DI
00886333207008 FDA UDI
510(k) Number
K915301 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Fluid transfer set, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 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

Yes

FDA UDI

Category: Fluid transfer set, general-purpose

Manifold by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluid transfer set, general-purpose.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e61d4cd6-8b7d-49d3-9993-b530de19dbae 37 fields · synced Jun 9, 2026