What is FDA product code CAZ?

This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

Anesthesia Conduction Kit → Anesthesiology

Name: Anesthesia Conduction Kit
Brand: Anesthesia Conduction Kit

1manufacturer

16catalogue 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 Anesthesia Conduction Kit
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	2016-09-16
Record revised	2025-08-07 (version 7)

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	Storage environment temperature 20 to 25 °C; Special storage condition: Do not freeze
Packaging	Case of 10, pack or inner pack of 100
Distribution end date	2020-09-17
UDI direct marking	Exempt

Catalogue Numbers

Catalogue numbers for Anesthesia Conduction Kit
Catalogue number	Per pack	Status
405658	10	In distribution
405721	10	In distribution
403250		In distribution
405663	10	In distribution
405723	10	In distribution
406008		Withdrawn
406006		Withdrawn
405641		Withdrawn
405676		Withdrawn
406030		Withdrawn
406055		Withdrawn
405690		Withdrawn
406077		Withdrawn
406138		Withdrawn
406056		Withdrawn
406025		Withdrawn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

Recalls Naming This Product

2 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Anesthesia Conduction Kit
Recalled by	Identified by	Initiated	FDA class	Root cause	Reason	Quantity
Becton, Dickinson & Co.	UDI-DI	2026-04-27	Class I	Nonconforming Material/Component	This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing s	150 units
Becton, Dickinson & Co.	UDI-DI	2026-04-27	Class I	Nonconforming Material/Component	This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing s	13,320 units

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.

Anesthesia Conduction Kit