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BD Oral Syringe

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Oral Syringe FDA UDI
Generic Name
Non-ISO80369-3-standardized oral syringe FDA UDI
Device Name
SYRINGE ORAL 3ML CLEAR FDA UDI
Model / Reference
305220 FDA UDI
Description
SYRINGE ORAL 3ML CLEAR FDA UDI

Identifiers

Catalog Number
305220 FDA UDI
Primary DI / UDI-DI
30382903052203 FDA UDI
FDA Product Code
KYW FDA UDI
GMDN Term
Non-ISO80369-3-standardized oral syringe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI

Category: Non-ISO80369-3-standardized oral syringe

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

Similar devices

Also classified as Non-ISO80369-3-standardized oral syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI 8fe0d82d-ccbf-4c81-bb3d-359d21d6b0bb 36 fields · synced May 31, 2026