Munevo Drive
munevo Drive: 1 catalogue number listed by Munevo Gmbh, Germany, under Components, Wheelchair. 54 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jiangsu (18), Guangdong (14), Zhejiang (11). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Kunshan Hi-Fortune Health Products Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 32 |
| Chiaphua Components (Jiangxi) Limited | Yichun | Jiangxi | Contract manufacturer | 23 |
| Feishen Group Co., Ltd. | Yongkang | Zhejiang | Contract manufacturer | 22 |
| Guangdong Marshell Electric Vehicle Co., Ltd. | Zhaoqing | Guangdong | Contract manufacturer | 22 |
| Jiangyin Huashi Medical Equipment Co., Ltd. | Jiangyin | Jiangsu | Contract manufacturer | 21 |
| Zhenjiang Assure Medical Equipment Co Ltd | Zhenjiang | Jiangsu | Contract manufacturer | 18 |
| Jiangsu Yuyue Medical Equipment & Supply Company Limited | Jiangsu | Jiangsu | Contract manufacturer | 17 |
| Raise Medical Industries, Inc. | Foshan | Guangdong | Contract manufacturer | 16 |
| Permobil Trading (Kunshan) Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 8 |
| Three Bears (Jiangsu) Healthcare Technology Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 6 |
| Irest Health Science AND Technology Co., Ltd. | Jiaxing | Zhejiang | Contract manufacturer | 5 |
| Zhejiang Linix Motor Co., Ltd. | Dongyang | Zhejiang | Contract manufacturer | 4 |
Showing 12 of 54. All 54 manufacturers in China registered for Components, Wheelchair
Record
| Listed by | Munevo Gmbh, Germany |
|---|---|
| FDA product code | KNN |
| Device type | Components, Wheelchair |
| Device class | Class 1 |
| Regulation | 21 CFR 890.3920 |
| Establishment | Complaint-file establishment, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2023-11-02 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | lot or batch number, manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| V2 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Action® | Action Products, Inc. | 233 |
| Axiom | Ki Mobility | 182 |
| Spex Limited | Spex Ltd | 132 |
| mo-Vis | MO-VIS BV | 123 |
| Medline | Medline Industries, Inc. | 111 |
| Everest & Jennings | GF Health Products, Inc | 108 |
| Spex | Spex Ltd | 70 |
| Drive | Drive DeVilbiss Healthcare | 36 |
| Evermed | Xiamen Taft Medical Co., Ltd. | 30 |
| Drivemedical | Drive DeVilbiss Healthcare | 24 |
| Cardinal Health | Cardinal Health 200, LLC | 23 |
| CoMoveIT | Comoveit | 8 |
Showing 12 of 159. All products under Components, Wheelchair
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 |
|---|---|---|---|---|---|---|
| Munevo Gmbh | UDI-DI | 2026-06-19 | Class II | Software Design Change | A software issue may cause the wheelchair’s driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift or imprecise control while driving the wheelchair. The wheelchair may veer from | 19 |
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.