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Bact/Alert® 3d Control Module

FDA UDI

Class I (US FDA UDI)

by Biomerieux , Inc.

Identity

Trade Name
BACT/ALERT® 3D CONTROL MODULE FDA UDI
Generic Name
Blood culture analyser IVD FDA UDI
Device Name
The BacT/ALERT 3D Control Module enables up to 6 incubator modules to be operated from one integrated touchscreen computer. FDA UDI
Model / Reference
210147 FDA UDI
Description
The BacT/ALERT 3D Control Module enables up to 6 incubator modules to be operated from one integrated touchscreen computer. FDA UDI

Identifiers

Primary DI / UDI-DI
03573026049522 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 Control 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 a78087a5-fd05-4219-97f6-13c2ad073498 35 fields · synced Jun 8, 2026