BD Luer-Lok

Tray SPN QNKE22G3.5 B/PI X3583B

Registry build 21.09.26
1manufacturer
5catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code CAZ
Manufacturer City Province Registered as Device types
Jiangsu Caina Medical Co., Ltd. Jiangyin Jiangsu Contract manufacturer 20

Record

Regulatory record for BD Luer-Lok
Listed by Becton, Dickinson AND Company, United States
FDA product code CAZ
Device type Anesthesia Conduction Kit
Device class Class 2
Regulation 21 CFR 868.5140
Establishment Contract manufacturer, Contract steriliser, Specification developer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2016-10-20
Record revised 2025-08-07 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Storage Special storage condition: Room Temperature
Packaging Case of 10
Distribution end date 2020-09-17
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for BD Luer-Lok
Catalogue number Size Per pack Status
405727 10 In distribution
405904 In distribution
408501 Withdrawn
405717 Withdrawn
405694 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Portex ICU Medical, Inc 1,340
Arrow Teleflex Medical LLC 508
Halyard Avanos Medical, Inc. 422
Avanos Avanos Medical, Inc. 315
Busse Hospital Disposables Robert Busse & Co., Inc. 215
Integra® Integra Pain Management 181
Epilong Pajunk Gmbh Medizintechnologie 79
BD Perisafe, BD Epilor, BD Luer-Lok Becton, Dickinson AND Company 44
Temena Temena GmbH 44
BD Luer-Lok, BD Glaspak Becton, Dickinson AND Company 36
Contiplex® B. Braun Medical Inc. 34
Stimulong Sono Pajunk Gmbh Medizintechnologie 27

Showing 12 of 109. All products under Anesthesia Conduction Kit

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K210983 2022-05-19

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer