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Rapid Infuser RI-2, 120V, 750 ml/min

FDA UDI

Class II (US FDA UDI)

by Belmont Instrument Corp.

Identity

Trade Name
Rapid Infuser RI-2, 120V, 750 ml/min FDA UDI
Generic Name
Warming/high-flow infusion pump FDA UDI
Model / Reference
903-00039 FDA UDI

Identifiers

Primary DI / UDI-DI
10896128002760 FDA UDI
510(k) Number
K242735 FDA UDI
FDA Product Code
LGZ FDA UDI
FRN FDA UDI
GMDN Term
Warming/high-flow infusion pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Warming/high-flow infusion pump

Rapid Infuser RI-2, 120V, 750 ml/min by Belmont Instrument Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Warming/high-flow infusion pump.

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 79f1eb3e-c4b1-46fe-a2ca-2147875df290 33 fields · synced May 30, 2026