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BD Safety-Lok

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Safety-Lok FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
SYRINGE SAFETYLOK 5ML LL FDA UDI
Model / Reference
305558 FDA UDI
Description
SYRINGE SAFETYLOK 5ML LL FDA UDI

Identifiers

Catalog Number
305558 FDA UDI
Primary DI / UDI-DI
30382903055587 FDA UDI
510(k) Number
K944757 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose syringe, single-use

BD Safety-Lok by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5cb98e5f-065a-472f-b171-84713c544422 35 fields · synced May 30, 2026