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BD Luer-Lok, BD Glaspak

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Luer-Lok, BD Glaspak FDA UDI
Generic Name
Intrathecal anaesthesia set, non-medicated FDA UDI
Device Name
TRAY SPN WHIT22G3.5 L/B-D/E FDA UDI
Model / Reference
405645 FDA UDI
Description
TRAY SPN WHIT22G3.5 L/B-D/E FDA UDI

Identifiers

Catalog Number
405645 FDA UDI
Primary DI / UDI-DI
50382904056457 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Intrathecal anaesthesia set, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 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

Yes

FDA UDI

Combination Product

Yes

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: Intrathecal anaesthesia set, non-medicated

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

Similar devices

Also classified as Intrathecal anaesthesia set, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0d9112eb-025b-492d-ac2b-425c64768034 35 fields · synced Jun 6, 2026