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Bact/Alert® Sa

FDA UDI

Class I (US FDA UDI)

by Biomerieux , Inc.

Identity

Trade Name
BACT/ALERT® SA FDA UDI
Generic Name
Basic/simple nutrient broth culture medium IVD FDA UDI
Device Name
The BACT/ALERT SA Culture Bottles are used for the recovery and detection of aerobic microorganisms (bacteria and fungi) from blood and other normally sterile body fluids. FDA UDI
Model / Reference
BACT/ALERT® SA FDA UDI
Description
The BACT/ALERT SA Culture Bottles are used for the recovery and detection of aerobic microorganisms (bacteria and fungi) from blood and other normally sterile body fluids. FDA UDI

Identifiers

Primary DI / UDI-DI
03573026595739 FDA UDI
510(k) Number
K020931 FDA UDI
FDA Product Code
MDB FDA UDI
GMDN Term
Basic/simple nutrient broth culture medium 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic/simple nutrient broth culture medium IVD

Bact/Alert® Sa by Biomerieux , Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic/simple nutrient broth culture medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomerieux , Inc.

Sources (1)

  • FDA UDI 7c2e4ae1-b45e-4d65-8365-9b5c6fb84f79 35 fields · synced Jun 6, 2026