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BD Dispenstirs™

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Dispenstirs™ FDA UDI
Generic Name
Treponema pallidum reagin antibody IVD, kit, agglutination FDA UDI
Device Name
BD Dispenstirs™ (single use, plastic pipettes), 0.05 mL, Box of 500 FDA UDI
Model / Reference
272905 FDA UDI
Description
BD Dispenstirs™ (single use, plastic pipettes), 0.05 mL, Box of 500 FDA UDI

Identifiers

Catalog Number
272905 FDA UDI
Primary DI / UDI-DI
30382902729052 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Treponema pallidum reagin antibody IVD, kit, agglutination FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Treponema pallidum reagin antibody IVD, kit, agglutination

BD Dispenstirs™ by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Treponema pallidum reagin antibody IVD, kit, agglutination.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 995ee5b4-cedc-47dc-a5ce-aadf6a0b3519 36 fields · synced May 30, 2026