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Riva

FDA UDI

Class II (US FDA UDI)

by ARxIUM, INC.

Identity

Trade Name
RIVA FDA UDI
Generic Name
Peripheral intravenous catheterization support kit FDA UDI
Device Name
A device used to prepare IV bags and syringes for hospital and compounding pharmacies. FDA UDI
Model / Reference
100000 FDA UDI
Description
A device used to prepare IV bags and syringes for hospital and compounding pharmacies. FDA UDI

Identifiers

Catalog Number
CON-0100-9 FDA UDI
Primary DI / UDI-DI
00691794010001 FDA UDI
FDA Product Code
NEP FDA UDI
GMDN Term
Peripheral intravenous catheterization support kit 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Peripheral intravenous catheterization support kit

Riva by ARxIUM, INC. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral intravenous catheterization support kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ARxIUM, INC.

Sources (1)

  • FDA UDI 815ac811-39b4-4a6e-9d74-0aacfb7442c2 36 fields · synced May 30, 2026