Hemodrop Blood Dispenser
Catalogue number BMP-HEMODROP, listed by Biomedical Polymers, Inc., United States, under Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use. 72 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jiangsu (17), Zhejiang (15), Guangdong (13). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Hangzhou Rollmed Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 127 |
| Jiangsu Kangjian Medical Apparatus Co., Ltd. | Jiangyan | Jiangsu | Contract manufacturer | 19 |
| Yancheng Huida Medical Instruments Co., Ltd. | Yancheng | Jiangsu | Contract manufacturer | 10 |
| Yantai Addcare Bio-Tech Co., Ltd. | Yantai | Shandong | Contract manufacturer | 8 |
| HUA Cheng XIN Plastic Mold Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 5 |
| Guangzhou Komaspec Mechanical AND Electrical Products Manufa | Huashan Town, Huadu District | Guangdong | Contract manufacturer | 4 |
| Inplast Plastic & Electronics Co., Ltd. | Suzhou New District | Jiangsu | Contract manufacturer | 2 |
| Flextronics Medical Molding (Shenzhen) Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 1 |
| Boen Healthcare Co., Ltd. | Suzhou | Jiangsu | Specification developer | 263 |
| Debo Medical Technology (Shijiazhuang) Co., Ltd. | Shijiazhuang | Hebei | Contract manufacturer | 117 |
| Zhejiang Mediunion Healthcare Group Co., Ltd. | Ningbo | Zhejiang | Contract manufacturer | 105 |
| Zhejiang Orient Gene Biotech | Huzhou | Zhejiang | Contract manufacturer | 86 |
Showing 12 of 72. All 72 manufacturers in China registered for Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
Record
| Listed by | Biomedical Polymers, Inc., United States |
|---|---|
| FDA product code | LXG |
| Device type | Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use |
| Device class | Class 1 |
| Regulation | 21 CFR 862.2050 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2023-08-22 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Latex | Labelled latex-free |
| Packaging | Inner case of 1000, case of 27 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| BMP-HEMODROP | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Globe Scientific | Globe Scientific, LLC | 144 |
| Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use | Scientific Device Laboratory, Inc. | 61 |
| Gongdong | Zhejiang Gongdong Medical Technology Co., Ltd. | 26 |
| Cardinal Health | Cardinal Health 200, LLC | 24 |
| De-/Recapper 900 Flex ID, 115V | Sarstedt Aktiengesellschaft & Co.KG | 20 |
| CellSHILED | Equashield Medical Ltd | 19 |
| Porex SQ-Easy | Porex Corporation | 17 |
| Corning | Corning Incorporated | 15 |
| Pathfinder | AIM LAB Automation Technologies PTY Ltd | 15 |
| Yingtai | Changsha Yingtai Instrument Co., Ltd. | 13 |
| Helmer Scientific | Helmer Inc. | 12 |
| Kbmed | KB Medical (Group) Inc. | 11 |
Showing 12 of 424. All products under Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
Recalls
2 of these are Class III. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2019-09-18 | Class III | Component change control | The metal cannula of the device either broke and the broken piece left in the blood specimen tube, or slid back into the plastic portion of the device instead of piercing the tube. | 2,052,000 | 2020-09-15 |
| 2019-09-18 | Class III | Component change control | The metal cannula of the device either broke and the broken piece left in the blood specimen tube, or slid back into the plastic portion of the device instead of piercing the tube. | 108,000 | 2020-09-15 |
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.