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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
Biological sterilization indicator FDA UDI
Device Name
20 Minute Biological Indicator, 25 Count FDA UDI
Model / Reference
RR20BI FDA UDI
Description
20 Minute Biological Indicator, 25 Count FDA UDI

Identifiers

Primary DI / UDI-DI
10889950139889 FDA UDI
510(k) Number
K181686 FDA UDI
FDA Product Code
FRC FDA UDI
GMDN Term
Biological sterilization indicator 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Biological sterilization indicator

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 Biological sterilization indicator.

Cleared under the same submission

K181686 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 91162a62-264c-411a-b824-730375ecd812 35 fields · synced May 30, 2026