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Bact/Alert® 3d Right Incubation Module

FDA UDI

Class I (US FDA UDI)

by Biomerieux , Inc.

Identity

Trade Name
BACT/ALERT® 3D RIGHT INCUBATION MODULE FDA UDI
Generic Name
Blood culture analyser IVD FDA UDI
Device Name
The BacT/ALERT 3D Right Incubator Module has four independent drawers of 60 cells each. Patented cell flags track bottle movements between cells for greater ease of use. FDA UDI
Model / Reference
210161 FDA UDI
Description
The BacT/ALERT 3D Right Incubator Module has four independent drawers of 60 cells each. Patented cell flags track bottle movements between cells for greater ease of use. FDA UDI

Identifiers

Primary DI / UDI-DI
03573026049591 FDA UDI
510(k) Number
K903505 FDA UDI
K981736 FDA UDI
FDA Product Code
MDB FDA UDI
GMDN Term
Blood culture analyser IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2560 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

No

FDA UDI

Category: Blood culture analyser IVD

Bact/Alert® 3d Right Incubation Module by Biomerieux , Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood culture analyser IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomerieux , Inc.

Sources (1)

  • FDA UDI 46768a08-c757-42ae-a7b0-81f3a2828a68 35 fields · synced Jun 6, 2026