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BD BACTEC™ Subculturing/Aerobic Venting Unit

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD BACTEC™ Subculturing/Aerobic Venting Unit FDA UDI
Generic Name
Syringe/blood collection tube adaptor IVD FDA UDI
Device Name
BD BACTEC™ Subculturing/Aerobic Venting Unit (50 per carton) FDA UDI
Model / Reference
249560 FDA UDI
Description
BD BACTEC™ Subculturing/Aerobic Venting Unit (50 per carton) FDA UDI

Identifiers

Catalog Number
249560 FDA UDI
Primary DI / UDI-DI
30382902495605 FDA UDI
FDA Product Code
JTA FDA UDI
GMDN Term
Syringe/blood collection tube adaptor 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Syringe/blood collection tube adaptor IVD

BD BACTEC™ Subculturing/Aerobic Venting Unit by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Syringe/blood collection tube adaptor IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ccd78489-db94-4483-a1eb-9084b82d0166 36 fields · synced May 29, 2026