← Back to catalogue

BD Sputum Collection System

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Sputum Collection System FDA UDI
Generic Name
Oral/respiratory tract specimen container IVD, no additive/medium FDA UDI
Device Name
BD Sputum Collection System, Case of 72 units FDA UDI
Model / Reference
290020 FDA UDI
Description
BD Sputum Collection System, Case of 72 units FDA UDI

Identifiers

Catalog Number
290020 FDA UDI
Primary DI / UDI-DI
30382902900208 FDA UDI
FDA Product Code
JTW FDA UDI
GMDN Term
Oral/respiratory tract specimen container IVD, no additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2900 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Oral/respiratory tract specimen container IVD, no additive/medium

BD Sputum Collection System by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oral/respiratory tract specimen container IVD, no additive/medium.

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
Becton Dickinson And Company

Sources (1)

  • FDA UDI 525a029f-68ae-48e8-9711-1410bb216259 36 fields · synced Jun 8, 2026