Introcan Safety®
Introcan Safety® IV Catheter 24 Ga. x 0.55 in., FEP, Straight, Thinwall
13manufacturers in China registered for this device type
44catalogue numbers in this listing
9510(k) clearances naming this product code
Who Else Makes It
Concentrated in Jiangsu (5), Beijing (3), Shanghai (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Mehow Innovative (Huizhou) Ltd. | Huizhou | Guangdong | Contract manufacturer | 11 |
| Tianjin Demax Medical Technology Co., Ltd. | Tianjin | Tianjin | Contract manufacturer | 5 |
| Steris Sterilization Technologies (Suzhou) Ltd | Suzhou | Jiangsu | Contract manufacturer | 44 |
| Shanghai INT Medical Instruments Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 10 |
| Lepu Medical Technology (Beijing) Co., Ltd. | Beijing | Beijing | Manufacturer | 7 |
| Beijing Target Medical Technologies Inc. | Beijing | Beijing | Contract manufacturer | 7 |
| Beijing Demax Medical Technology Co., Ltd. | Beijing | Beijing | Manufacturer | 5 |
| Curatia Medical Limited | Suzhou | Jiangsu | Specification developer | 5 |
| Tianjin Ethylene Oxide Sterilization Technology Co., Ltd. | Tianjin | Tianjin | Contract manufacturer | 4 |
| Shanghai Microport EP Medtech Co., Ltd. | Shanghai | Shanghai | Manufacturer | 3 |
| Becton Dickinson Medical Devices Co., Ltd. Suzhou | Suzhou | Jiangsu | Contract manufacturer | 2 |
| Cardiocycle Medical(Suzhou) Co., Ltd. | Suzhou | Jiangsu | Complaint-file establishment | 1 |
Showing 12 of 13. All 13 manufacturers in China registered for Introducer, Catheter
Record
| Listed by | B. Braun Medical Inc., United States |
|---|---|
| FDA product code | DYB |
| Device type | Introducer, Catheter |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1340 |
| Establishment | Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer |
| Record published | 2016-09-23 |
| Record revised | 2022-06-10 (version 14) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: Keep away from sunlight; Special storage condition: Keep dry |
| Packaging | Carton of 4 |
| Distribution end date | 2020-06-01 |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| 4253612-02 | Catheter-Gauge : 16 | 50 | In distribution |
| 4251611-02 | Catheter-Gauge : 24 | 50 | In distribution |
| 4251890-02 | Catheter-Gauge : 14 | 50 | In distribution |
| 4252500-02 | Catheter-Gauge : 24 | 50 | In distribution |
| 4252578-02 | Catheter-Gauge : 16 | 50 | In distribution |
| 4251607-02 | Catheter-Gauge : 24 | 50 | In distribution |
| 4254562-020 | Catheter-Gauge : 18 | 50 | In distribution |
| 4254512-02 | Catheter-Gauge : 24 | 50 | In distribution |
| 4252594-020 | Catheter-Gauge : 14 | 50 | In distribution |
| 4251870-020 | Catheter-Gauge : 14 | 50 | In distribution |
| 4253566-02 | Catheter-Gauge : 20 | 50 | In distribution |
| 4251611-020 | Catheter-Gauge : 24 | 50 | In distribution |
| 4252586-020 | Catheter-Gauge : 16 | 50 | In distribution |
| 4254503-02 | Catheter-Gauge : 24 | 50 | In distribution |
| 4254562-02 | Catheter-Gauge : 18 | 50 | In distribution |
| 4252561-02 | Catheter-Gauge : 18 | 50 | In distribution |
| 4253590-02 | Catheter-Gauge : 18 | 50 | In distribution |
| 4254570-02 | Catheter-Gauge : 16 | 50 | In distribution |
| 4254512-020 | Catheter-Gauge : 24 | 50 | In distribution |
| 4251717-02 | Catheter-Gauge : 14 | 50 | In distribution |
| 4252551-020 | Catheter-Gauge : 18 | 50 | In distribution |
| 4251614-02 | Catheter-Gauge : 24 | 50 | In distribution |
| 4252536-020 | Catheter-Gauge : 20 | 50 | In distribution |
| 4251620-02 | Catheter-Gauge : 18 | 50 | In distribution |
| 4252500-020 | Catheter-Gauge : 24 | 50 | In distribution |
| 4252543-02 | Catheter-Gauge : 20 | 50 | In distribution |
| 4254538-020 | Catheter-Gauge : 20 | 50 | In distribution |
| 4253540-02 | Catheter-Gauge : 22 | 50 | In distribution |
| 4251679-02 | Catheter-Gauge : 18 | 50 | In distribution |
| 4253523-02 | Catheter-Gauge : 24 | 50 | In distribution |
| 4252560-020 | Catheter-Gauge : 18 | 50 | In distribution |
| 4254546-02 | Catheter-Gauge : 20 | 50 | In distribution |
| 4251628-02 | Catheter-Gauge : 22 | 50 | In distribution |
| 4252551-02 | Catheter-Gauge : 18 | 50 | In distribution |
| 4252535-020 | Catheter-Gauge : 20 | 50 | In distribution |
| 4251644-020 | Catheter-Gauge : 20 | 50 | In distribution |
| 4251709-020 | Catheter-Gauge : 16 | 50 | In distribution |
| 4251687-02 | Catheter-Gauge : 18 | 50 | In distribution |
| 4252586-02 | Catheter-Gauge : 16 | 50 | In distribution |
| 4251601-02 | Catheter-Gauge : 24 | 50 | In distribution |
| 4251628-020 | Catheter-Gauge : 22 | 50 | In distribution |
| 4253511-02 | Catheter-Gauge : 24 | 50 | In distribution |
| 4251609-02 | Catheter-Gauge : 24 | 50 | Withdrawn |
| 4251612-02 | Catheter-Gauge : 24 | 50 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Demax | Beijing Demax Medical Technology Co., Ltd. | 2,841 |
| Arrow | Teleflex Medical LLC | 1,036 |
| Prelude IDeal™ | Merit Medical Systems, Inc. | 294 |
| Fast-Cath™ | St. Jude Medical | 213 |
| Flexor | Cook Incorporated | 182 |
| Prelude Ease™ | Merit Medical Systems, Inc. | 176 |
| Performer | Cook Incorporated | 174 |
| VSI | Teleflex Medical LLC | 154 |
| Peel-Away | Cook Incorporated | 153 |
| OptiSeal™ | Greatbatch Medical | 127 |
| Brilliant | Lepu Medical Technology (Beijing) Co., Ltd. | 122 |
| Super Sheath | Togo Medikit Co., Ltd. | 122 |
Showing 12 of 439. All products under Introducer, Catheter
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K033527 | 2004-02-05 |
| K030135 | 2003-07-15 |
| K021094 | 2002-07-03 |
| K961745 | 1996-09-17 |
| K960406 | 1996-04-12 |
| K955820 | 1996-03-25 |
| K945396 | 1995-03-13 |
| K931743 | 1993-11-02 |
| K930057 | 1993-08-06 |
Recalls Naming This Product
1 recall names this product by its own identifier, the UDI on its label.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| B. Braun Medical Inc. | UDI-DI | 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.