Centurion
ST. STR Mosquito Hemostat 3 1/2'(MHB700)
12manufacturers in China registered for this device type
28catalogue numbers in this listing
Who Else Makes It
Concentrated in Jiangsu (4), Shandong (3), Shanghai (2). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| B.Braun Medical (Suzhou) Co,.Ltd | Suzhou | Jiangsu | Contract manufacturer | 37 |
| Shanghai Medical Instruments (Group) Ltd. Corp. | Shanghai | Shanghai | Contract manufacturer | 235 |
| Xinhua Surgical Instrument Co., Ltd. | Zibo | Shandong | Manufacturer | 222 |
| Shandong Zhushi Pharmaceutical Group Co., Ltd. | Heze | Shandong | Contract manufacturer | 65 |
| Weihai Hongyu Nonwoven Fabric Products Co., Ltd. | Weihai | Shandong | Contract manufacturer | 37 |
| Shanghai Wilpower Industrial Co., Ltd. | Shanghai | Shanghai | Exporter | 33 |
| H&K International Trade Limited (China) | Jinhua | Zhejiang | Contract manufacturer | 29 |
| Hangzhou Haizhu MIM Products Co., Ltd. | Hangzhou | Zhejiang | Exporter | 28 |
| Bothwin (Beijing) Medical Technology Co., Ltd. | Beijng | Beijing | Manufacturer | 25 |
| Suzhou Virgil Medical Technology Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 20 |
| Huaian Frimen Co., Ltd. | Huaian | Jiangsu | Manufacturer | 16 |
| Huaian Wolfram Surgical Instruments | Huaian | Jiangsu | Manufacturer | 14 |
Record
| Listed by | Centurion Medical Products Corporation, United States |
|---|---|
| FDA product code | HRQ |
| Device type | Hemostat |
| Device class | Class 1 |
| Regulation | 21 CFR 878.4800 |
| Premarket notification | Exempt |
| Record published | 2021-12-31 |
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 |
| Packaging | Case of 20, case of 500, box of 20 |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 67655 | In distribution | |
| 66170K | In distribution | |
| 66145 | In distribution | |
| I68310 | In distribution | |
| 66695 | In distribution | |
| 67140 | In distribution | |
| 66485 | In distribution | |
| MHS102SMB | In distribution | |
| 67330K | In distribution | |
| 66145K | In distribution | |
| 67325 | In distribution | |
| I68100 | In distribution | |
| TRI66140 | In distribution | |
| 67330 | In distribution | |
| 66175K | In distribution | |
| 67330K | In distribution | |
| 66445 | In distribution | |
| MHS103MB | In distribution | |
| 65240 | In distribution | |
| 65340 | In distribution | |
| 66145K | In distribution | |
| 66695K | In distribution | |
| 67660 | In distribution | |
| 65240 | In distribution | |
| I68155 | In distribution | |
| 66175 | In distribution | |
| 66170 | In distribution | |
| TRI66765 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Medicon | Medicon eG. Chirurgiemechaniker-Genossenschaft | 429 |
| Integra® Miltex® | Integra LifeSciences Production Corporation | 249 |
| Integra® Jarit® | Integra LifeSciences Production Corporation | 231 |
| Aesculap | Aesculap AG | 183 |
| Boss Instruments | Boss Instruments, Ltd. | 182 |
| Assi | Accurate Surgical & Scientific Instruments Corp. | 164 |
| BR Surgical, LLC | BR Surgical LLC | 123 |
| Hayden Medical | Hayden Medical Inc | 93 |
| Surgipros | Surgipros LLC | 71 |
| Pilling | Teleflex Medical LLC | 70 |
| V. Mueller | Steris Corporation | 41 |
| Cardinal Health | Cardinal Health 200, LLC | 39 |
Showing 12 of 92. All products under Hemostat
Recalls Naming This Product
2 recalls name this product by its own identifiers, the UDI on its label.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Medline Industries, LP – Northfield | UDI-DI | 2024-11-12 | Class II | Process control | Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection. | 21,440 total |
| Medline Industries, LP – Northfield | UDI-DI | 2024-02-23 | Class II | Process control | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. | 80903 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.