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Manifold

FDA UDI

Class II (US FDA UDI)

by Valflux Group, Llc

Identity

Trade Name
MANIFOLD FDA UDI
Generic Name
Contrast medium injection system administration set FDA UDI
Device Name
VGAM0201 MANIFOLD FDA UDI
Model / Reference
VGAM0201 FDA UDI
Description
VGAM0201 MANIFOLD FDA UDI

Identifiers

Catalog Number
VGAM0201 FDA UDI
Primary DI / UDI-DI
00850004162019 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Contrast medium injection system administration set 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Contrast medium injection system administration set

Manifold by Valflux Group, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Contrast medium injection system administration set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Valflux Group, Llc

Sources (1)

  • FDA UDI dd36b32d-6e04-4c38-933f-a2e03fb2f174 35 fields · synced May 30, 2026