ClosureFast™
Catheter CF7-7-100 Closure Fast V03
65manufacturers in China registered for this device type
12catalogue numbers in this listing
6510(k) clearances naming this product code
Who Else Makes It
Concentrated in Guangdong (24), Zhejiang (13), Shanghai (10). 23 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 77 |
| Shandong Weigao Orthopaedic Device Co., Ltd. | Weihai | Shandong | Contract manufacturer | 42 |
| Hangzhou Kangji Medical Instrument Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 27 |
| Modern Medical Equipment Manufacturing Ltd. | Heng Li, Dongguan | Guangdong | Contract manufacturer | 26 |
| Amphenol Alden Products Company | Shenzhen | Guangdong | Contract manufacturer | 24 |
| Hangzhou Endo Medical Instrument Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 19 |
| Hong Qiangxing (Shen Zhen) Electronics Limited | Shenzhen | Guangdong | Contract manufacturer | 19 |
| Shenzhen MED-Link Electronics Tech Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 18 |
| Sanbor Medical Xiamen, Inc. | Xiamen | Fujian | Contract manufacturer | 16 |
| ATL Technology DG,Ltd. | Dongguan | Guangdong | Contract manufacturer | 14 |
| Jiangyin Sinbon Electronics Co Ltd | Jiangyin | Jiangsu | Contract manufacturer | 13 |
| Guangzhou Huada Biotechnology Co., Ltd. | Guangzhou | Guangdong | Contract manufacturer | 9 |
Showing 12 of 65. All 65 manufacturers in China registered for Electrosurgical, Cutting & Coagulation & Accessories
Record
| Listed by | Medtronic, Inc., United States |
|---|---|
| FDA product code | GEI |
| Device type | Electrosurgical, Cutting & Coagulation & Accessories |
| Device class | Class 2 |
| Regulation | 21 CFR 878.4400 |
| Establishment | Specification developer, Repacker / relabeller, Manufacturer, Exporter |
| 510(k) | K111887 |
| Record published | 2017-05-14 |
| Record revised | 2019-03-11 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number |
| Storage | Storage environment temperature -29 to 60 °C; Storage environment humidity 15 to 90 % RH |
| Sizes | Outer diameter 2.3 mm; catheter gauge 7 Fr; length 3 to 100 cm |
| Distribution end date | 2018-10-05 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| CF7-3-60 | Introducer sheath: 7 Fr | In distribution |
| CF6-8-100 | Insertable length: 100 cm | In distribution |
| CF7-7-60 | Heating Element Length 7 CM | In distribution |
| CF7-7-60 | Length 7.0 cm | In distribution |
| CF7-7-100 | Length 7.0 cm | In distribution |
| CF6-8-60 | Heating element diameter: 2.0 mm | In distribution |
| CF7-3-60 | Outer Diameter 2.3 mm | Withdrawn |
| CF7-7-60 | Catheter Gauge 7.0 Fr | Withdrawn |
| CF7-3-60 | Outer Diameter 2.3 mm | Withdrawn |
| CF7-7-60 | Catheter Gauge 7.0 Fr | Withdrawn |
| CF7-7-100 | Working Length 100 CM | Withdrawn |
| CF7-7-100 | Heating Element Length 7 CM | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Surgical Direct | Surgical Direct, Inc. | 5,729 |
| Speedlock | National Advanced Endoscopy Devices, Inc. | 5,212 |
| Stingray Surgical Products | Stingray Surgical Products L.L.C. | 4,647 |
| Kirwan | Kirwan Surgical Products, LLC. | 1,901 |
| Millennium | Avalign Technologies, Inc. | 1,779 |
| DANmed | Dannoritzer Medizintechnik GmbH & Co. KG | 1,590 |
| Elmed | Elmed, Inc. | 1,519 |
| Symmetry Olsen | Aspen Surgical Products, Inc. | 1,219 |
| Guenter Bissinger Medizintechnik GmbH | Günter Bissinger Medizintechnik GmbH | 1,117 |
| Ambler Surgical | Ambler Surgical, LLC | 756 |
| V. Mueller | Steris Corporation | 661 |
| Aesculap | Aesculap AG | 544 |
Showing 12 of 2,922. All products under Electrosurgical, Cutting & Coagulation & Accessories
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K223488 | 2023-03-23 |
| K113380 | 2012-11-15 |
| K121290 | 2012-06-25 |
| K120537 | 2012-05-10 |
| K093203 | 2010-02-26 |
| K060400 | 2006-02-28 |
Recalls Naming This Product
2 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Vnus Medical Technologies, Inc. | 510(k) number | 2007-08-08 | Not classified | Labeling design | Instructions for Use change: Instructions for Use have been changed to include a modified placement recommendation. | 16,716 units | 2008-05-22 |
| Vnus Medical Technologies, Inc. | 510(k) number | 2007-03-06 | Not classified | Package design/selection | Sterility (package integrity) Compromised: Product sterility may be compromised due to a pinhole under the pouch foldover. | 92 units | 2007-12-17 |
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.