← Back to catalogue

BacT/ALERT® Blood Collection Adapter Cap

FDA UDI

Class II (US FDA UDI)

by Biomerieux , Inc.

Identity

Trade Name
BacT/ALERT® Blood Collection Adapter Cap FDA UDI
Generic Name
Blood collection tube holder, reusable FDA UDI
Device Name
The BacT/ALERT Blood Collection Adapter is used as an aid to facilitate filling of blood into the BacT/ALERT Blood Culture Bottle when using a blood collection set FDA UDI
Model / Reference
BacT/ALERT® Blood Collection Adapter Cap FDA UDI
Description
The BacT/ALERT Blood Collection Adapter is used as an aid to facilitate filling of blood into the BacT/ALERT Blood Culture Bottle when using a blood collection set FDA UDI

Identifiers

Primary DI / UDI-DI
03573026556105 FDA UDI
510(k) Number
K933939 FDA UDI
FDA Product Code
GIM FDA UDI
GMDN Term
Blood collection tube holder, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 FDA UDI
Commercial Distribution
Not 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

BacT/ALERT® Blood Collection Adapter Cap by Biomerieux , Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biomerieux , Inc.

Sources (1)

  • FDA UDI b0a6c328-a36b-41ed-88d7-c287cebca524 35 fields · synced Jun 8, 2026