Introcan Safety ® 2

Introcan Safety 2 is an over-the-needle peripheral intravenous catheter for short-term vascular access. Its radiopaque polyurethane catheter has an integrated septum and a passive needle…

Registry build 21.09.26

Introcan Safety 2 is an over-the-needle peripheral intravenous catheter for short-term vascular access. Its radiopaque polyurethane catheter has an integrated septum and a passive needle shield within the hub.

As the needle is withdrawn, the septum wipes its surface and seals after removal to contain blood. The shield automatically covers the needle tip during withdrawal and prevents reinsertion once engaged, providing protection during disposal.

Listed Item

Introcan Safety® 2 IV Catheter – 18 Ga. x 1.25 in.

Catheter Configurations

The family includes winged and wingless single-lumen catheters with tapered tips, in sizes from 18 to 24 gauge. Length options range from 14 to 50 mm. The filed 18 gauge, 1.25 inch catheter is one configuration. Intravascular power-injector use has a maximum pressure rating of 325 psi with a Luer-lock connection.

12manufacturers in China registered for this device type
35catalogue numbers in this listing
12510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Shandong (3), Guangdong (3), Jiangsu (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FOZ
Manufacturer City Province Registered as Device types
Amsino Medical (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 22
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8
Weihai Jierui Medical Products Co., Ltd. Weihai Shandong Contract manufacturer 3
Becton Dickinson Medical Devices Co., Ltd. Suzhou Suzhou Jiangsu Contract manufacturer 2
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Zhejiang Kindly Medical Devices Co., Ltd. Wenzhou Zhejiang Contract manufacturer 16
Terumo Medical Products (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Shandong Ande Healthcare Apparatus Co., Ltd. Zibo Shandong Manufacturer 7
Jiangxi Sanxin Medtec Co., Ltd. Nanchang Jiangxi Manufacturer 6
Haolang Technology (Foshan) Limited Corporation Foshan Guangdong Contract manufacturer 6
Guangdong Baihe Medical Technology Co., Ltd. Foshan Guangdong Contract manufacturer 4
Foshan Special Medical Co., Ltd. Foshan Guangdong Manufacturer 3

Record

Regulatory record for Introcan Safety ® 2
Listed by B. Braun Medical Inc., United States
FDA product code FOZ
Device type Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device class Class 2
Regulation 21 CFR 880.5200
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
510(k) K220756
Record published 2022-03-25
Record revised 2022-12-16 (version 3)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Carton of 4

Catalogue Numbers

Catalogue numbers for Introcan Safety ® 2
Catalogue number Size Per pack Status
4232008-02 Catheter-Gauge : 20 50 In distribution
4242013-02 Catheter-Gauge : 18 50 In distribution
4242015-02 Catheter-Gauge : 18 50 In distribution
4232006-02 Catheter-Gauge : 20 50 In distribution
4232015-02 Catheter-Gauge : 18 50 In distribution
4242012-02 Catheter-Gauge : 18 50 In distribution
4232012-02 Catheter-Gauge : 18 50 In distribution
4232003-02 Catheter-Gauge : 24 50 In distribution
4232013-02 Catheter-Gauge : 18 50 In distribution
4242009-02 Catheter-Gauge : 20 50 In distribution
4242025-02 50 In distribution
4232014-02 Catheter-Gauge : 18 50 In distribution
4232007-02 Catheter-Gauge : 20 50 In distribution
4232004-02 Catheter-Gauge : 22 50 In distribution
4242011-02 Catheter-Gauge : 20 50 In distribution
4242007-02 Catheter-Gauge : 20 50 In distribution
4242003-02 Catheter-Gauge : 24 50 In distribution
4242000-02 Catheter-Gauge : 24 50 In distribution
4232000-02 Catheter-Gauge : 24 50 In distribution
4232002-02 Catheter-Gauge : 24 50 In distribution
4242005-02 Catheter-Gauge : 22 50 In distribution
4242008-02 Catheter-Gauge : 20 50 In distribution
4242026-02 50 In distribution
4232005-02 Catheter-Gauge : 22 50 In distribution
4242024-02 50 In distribution
4242001-02 Catheter-Gauge : 24 50 In distribution
4232001-02 Catheter-Gauge : 24 50 In distribution
4242006-02 Catheter-Gauge : 20 50 In distribution
4232009-02 Catheter-Gauge : 20 50 In distribution
4242014-02 Catheter-Gauge : 18 50 In distribution
4242004-02 Catheter-Gauge : 22 50 In distribution
4242027-02 50 In distribution
4242010-02 Catheter-Gauge : 20 50 In distribution
4242028-02 50 In distribution
4242002-02 Catheter-Gauge : 24 50 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 2,368
Cook Cook Incorporated 250
Cook Spectrum Cook Incorporated 225
Jelco ICU Medical, Inc 104
Medline Medline Industries, Inc. 95
Deltaven Fast Flash Delta Med SpA 77
Deltaven Delta Med SpA 73
PowerGlide Pro Bard Access Systems, Inc. 63
Peripheral Catheter Insertion Kit Bard Access Systems, Inc. 62
Able Central Venous Catheter Guangdong Baihe Medical Technology Co., Ltd. 62
Curaplex Bound Tree Medical, LLC 61
BD Cathena™ Safety IV Catheter Becton, Dickinson AND Company 59

Showing 12 of 285. All products under Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253235 2026-05-15
K241845 2024-07-26
K220756 2022-06-23
K220626 2022-05-14
K213664 2022-02-11
K213085 2021-10-25
K192676 2020-04-01
K182870 2019-03-07
K023253 2003-05-06
K020785 2002-08-28
K982805 1999-01-14
K970736 1998-12-16

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2025-02-17 Class II Process control Increased risk for valve housing detachment causing leakage. 28,200 units
2022-09-01 Class II Process control Potential for leakage at the catheter hub. 94,000 US

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