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BioFire RP2.1/RP2.1plus Control Panel M441

FDA UDI

Class II (US FDA UDI)

by Mmqci

Identity

Trade Name
BioFire RP2.1/RP2.1plus Control Panel M441 FDA UDI
Generic Name
Multiple-genus respiratory virus nucleic acid IVD, control FDA UDI
Device Name
External quality controls to monitor the performance of in vitro laboratory nucleic acid testing procedures for the FilmArray RP2.1/ RP2.1plus assay on the FilmArray 2.0/Torch systems. FDA UDI
Model / Reference
v.00 FDA UDI
Description
External quality controls to monitor the performance of in vitro laboratory nucleic acid testing procedures for the FilmArray RP2.1/ RP2.1plus assay on the FilmArray 2.0/Torch systems. FDA UDI

Identifiers

Catalog Number
M441 FDA UDI
Primary DI / UDI-DI
00852720008114 FDA UDI
510(k) Number
K202196 FDA UDI
FDA Product Code
PMN FDA UDI
GMDN Term
Multiple-genus respiratory virus nucleic acid IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3920 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

Yes

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

No

FDA UDI

Category: Multiple-genus respiratory virus nucleic acid IVD, control

BioFire RP2.1/RP2.1plus Control Panel M441 by Mmqci — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-genus respiratory virus nucleic acid IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mmqci

Sources (1)

  • FDA UDI d7802ab3-feca-4072-a65b-b769c80ef3f7 37 fields · synced May 30, 2026