Tyshak II®
PDC534 20MM X 6CM Ball Cath Tysha II STD
5manufacturers in China registered for this device type
38catalogue numbers in this listing
Who Else Makes It
Concentrated in Jiangsu (3), Guangdong (2).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| OrbusNeich Medical (Shenzhen) Co., Ltd. | Shenzhen | Guangdong | Complaint-file establishment | 5 |
| Curatia Medical Limited | Suzhou | Jiangsu | Specification developer | 5 |
| Brosmed Medical Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 4 |
| Kossel Medtech (Suzhou) Co., Ltd. | Suzhou | Jiangsu | Manufacturer | 4 |
| DK Medical Technology Co., Ltd. | Suzhou | Jiangsu | Manufacturer | 3 |
Record
| Listed by | B. Braun Interventional Systems, Inc., United States |
|---|---|
| FDA product code | LIT |
| Device type | Catheter, Angioplasty, Peripheral, Transluminal |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1250 |
| 510(k) | K003052 |
| Record published | 2016-08-09 |
| Record revised | 2023-09-07 (version 8) |
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: Store at room temp; Special storage condition: Keep away from sunlight |
| Distribution end date | 2021-08-04 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 611535 | In distribution | |
| 611934 | In distribution | |
| 611946 | In distribution | |
| 611795 | In distribution | |
| 611693 | In distribution | |
| 611908 | In distribution | |
| 611921 | In distribution | |
| 611936 | In distribution | |
| 611949 | In distribution | |
| 611929 | In distribution | |
| 611909 | In distribution | |
| 611911 | In distribution | |
| 611913 | In distribution | |
| 611778 | In distribution | |
| 611531 | In distribution | |
| 611777 | In distribution | |
| 611920 | In distribution | |
| 611797 | In distribution | |
| 611915 | In distribution | |
| 611536 | In distribution | |
| 611948 | In distribution | |
| 611537 | In distribution | |
| 611935 | In distribution | |
| 611947 | In distribution | |
| 611912 | In distribution | |
| 611557 | In distribution | |
| 611796 | In distribution | |
| 611654 | Diameter (mm) : 13.000 MM | In distribution |
| 611781 | In distribution | |
| 611551 | In distribution | |
| 611553 | In distribution | |
| 611945 | In distribution | |
| 611918 | In distribution | |
| 611914 | In distribution | |
| 611926 | In distribution | |
| 611927 | In distribution | |
| 611772 | In distribution | |
| 611792 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Parafleet SC 018 PTA Balloon Dilatation Catheter | Brosmed Medical Co., Ltd. | 1,460 |
| Jade Plus PTA Balloon Dilatation Catheter / Jade Plus 18 OTW | OrbusNeich Medical (Shenzhen) Co., Ltd. | 832 |
| Jade PTA Balloon Dilatation Catheter | OrbusNeich Medical (Shenzhen) Co., Ltd. | 667 |
| Parafleet SC 014 PTA Balloon Dilatation Catheter | Brosmed Medical Co., Ltd. | 572 |
| Minerva PTA Balloon Dilatation Catheter | Brosmed Medical Co., Ltd. | 504 |
| Advocate | Arravasc, Ltd. | 441 |
| Ultraverse® 035 PTA Dilatation Catheter | Bard Peripheral Vascular, Inc. | 361 |
| Polux PTA Balloon Dilatation Catheter | Brosmed Medical Co., Ltd. | 359 |
| Advance | Cook Incorporated | 355 |
| Pacific™ Plus | Medtronic, Inc. | 347 |
| EverCross™ | ev3, Inc. | 316 |
| Achilles NC PTA Balloon Dilatation Catheter | Brosmed Medical Co., Ltd. | 297 |
Showing 12 of 167. All products under Catheter, Angioplasty, Peripheral, Transluminal
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Numed, Inc. | 510(k) number | 2009-09-23 | Not classified | Labeling design | The firm received a complaint from the sole direct account that while performing an inventory review it was observed that the packaging of the IMPACT catheter was cracked and deteriorating. The product was still in its packaging and never | 7,367 units domestically | 2012-05-23 |
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.