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ConFirm Rapid 20

FDA UDI

Class II (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
ConFirm Rapid 20 FDA UDI
Generic Name
Test tube heater FDA UDI
Device Name
20 Minute Reader Incubator FDA UDI
Model / Reference
RR20READER FDA UDI
Description
20 Minute Reader Incubator FDA UDI

Identifiers

Primary DI / UDI-DI
10889950139872 FDA UDI
510(k) Number
K233681 FDA UDI
FDA Product Code
FRC FDA UDI
GMDN Term
Test tube heater FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Test tube heater

ConFirm Rapid 20 by Hu-Friedy Mfg Co., Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Test tube heater.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 44de74b6-177f-4d8d-84a7-84dd02d74110 35 fields · synced May 30, 2026