Device, Patient Transfer, Powered
HoverMatt Half-Matt 39" W x 45 " L
27manufacturers in China registered for this device type
18catalogue numbers in this listing
1recall
Who Else Makes It
Concentrated in Guangdong (13), Jiangsu (5), Zhejiang (3). 2 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 |
| Hubei Yinkang Medical Equipment Co., Ltd. | Xiaogan | Hubei | Contract manufacturer | 8 |
| Gcmedica Enterprise Ltd.(Wuxi) | Wuxi | Jiangsu | Contract manufacturer | 55 |
| Dragon Medical Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 48 |
| Yearstar Healthcare Technology Co., Ltd. | Jiangyin | Jiangsu | Contract manufacturer | 43 |
| Foshan Fuzikon Medical Technology Co., Ltd. | Foshan | Guangdong | Manufacturer | 21 |
| Zhejiang Mateside Medical Devices Technology Co., Ltd. | Ningbo | Zhejiang | Contract manufacturer | 21 |
| Hebei Jiede Medical Equipment Co., Ltd. | Hengshui | Hebei | Contract manufacturer | 20 |
| Shenzhen Zhouyang Medical Care Product Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 18 |
| Metacare Industrial Ltd | Guangzhou | Guangdong | Contract manufacturer | 17 |
| Foshan Dahao Medical Technology Co., Ltd. | Foshan | Guangdong | Manufacturer | 13 |
| Zhongshan Juncheng Medical Technology Co., Ltd. | Zhongshan | Guangdong | Manufacturer | 12 |
Showing 12 of 27. All 27 manufacturers in China registered for Device, Patient Transfer, Powered
Record
| Listed by | Stryker Sustainability Solutions, United States |
|---|---|
| FDA product code | FRZ |
| Device type | Device, Patient Transfer, Powered |
| Device class | Class 2 |
| Regulation | 21 CFR 880.6775 |
| Establishment | Reprocessor, Specification developer, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2019-07-10 |
| Record revised | 2025-08-18 (version 6) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Prescription | Prescription only |
| Latex | Labelled latex-free |
| Label carries | lot or batch number |
| Packaging | Case of 10, case of 5 |
| Sizes | Width 34 to 50 in; length 45 to 81 in |
| Distribution end date | 2025-08-17 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| HM39RPSPU | Width 39.0 in | In distribution |
| HM39SPU | Length 78.0 in | In distribution |
| HM39SPU-LNK-B | Width 39.0 in | In distribution |
| R3242-RP | Width 39.0 in | In distribution |
| HM34SPU-HLF | Length 45.0 in | In distribution |
| HM39RPSPU-HLF | Width 39.0 in | In distribution |
| HM39SPU-B | Width 39.0 in | In distribution |
| HM34RPSPU-HLF | Length 45.0 in | In distribution |
| HM34RPSPU | Length 78.0 in | In distribution |
| HM34SPU | Width 34.0 in | In distribution |
| HM34SPU-HLF-B | Length 45.0 in | In distribution |
| HM39SPU-HLF-B | Length 45.0 in | In distribution |
| HM34SPU-B | Length 78.0 in | In distribution |
| HM50SPU | Width 50.0 in | In distribution |
| HM50SPU-B | Length 78.0 in | In distribution |
| HM34SPU-LNK-B | Length 78.0 in | In distribution |
| HM50RPSPU | Width 50.0 in | Withdrawn |
| HM39SPU-HLF | Length 45.0 in | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Zephyr Patient Positioning and Transfer System | Diacor, Inc. | 83 |
| Single Patient Use HoverMatt | Hovertech International | 38 |
| Sustainable Technologies | Cardinal Health 200, LLC | 21 |
| Hovertech | Hygia Health Services, Inc. | 19 |
| HoverMatt | Hovertech International | 11 |
| PremierPro Air Transfer Mats | Prestige Ameritech | 10 |
| Medline | Medline Industries, Inc. | 10 |
| Airpal | Caremed Supply, Inc. | 9 |
| HoverSling | Hovertech International | 6 |
| HoverTech Air Supply | Hovertech International | 6 |
| PPS Glide | Patient Positioning Systems, LLC | 6 |
| Alta | Qfix | 6 |
Showing 12 of 46. All products under Device, Patient Transfer, Powered
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 |
|---|---|---|---|---|---|---|
| Stryker Sustainability Solutions | UDI-DI | 2023-06-21 | Class II | Packaging process control | 39-inche-wide inflatable air transfer mattress packages contain 34-Inch-wide mattresses, so there may be a decreased surface area available to distribute the patient’s weight across, which may increase the effort exerted by staff for a late | 340 |
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.