CareLink
KIT MMT-7306 USB Carelink 2.4 RF Insert
Who Else Makes It
Concentrated in Guangdong (4), Shanghai (3), Jiangsu (2). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Edan Instruments, Inc. | Shenzhen | Guangdong | Contract manufacturer | 56 |
| Jabil Circuit (Shanghai) Ltd. | Shanghai | Shanghai | Contract manufacturer | 31 |
| Dongguan BAO Kang Dian ZI KE JI Limited | Dongguan | Guangdong | Contract manufacturer | 24 |
| Primecare Medical (Suzhou) Co., Ltd. | Changshu | Jiangsu | Contract manufacturer | 20 |
| Shenzhen Insighters Medical Technology Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 10 |
| Changshu Rozer Sterilization Technology Co., Ltd. | Changshu | Jiangsu | Contract manufacturer | 43 |
| Hangzhou Primecare Medical Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 29 |
| Shanghai Mediworks Precision Instruments Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 13 |
| Zhejiang Yigao Medical Technology Co., Ltd. | Hangzhou | Zhejiang | Manufacturer | 7 |
| Resvent Medical Technology Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 6 |
| Shanghai Draeger Medical Instrument Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 4 |
Record
| Listed by | Medtronic Minimed, United States |
|---|---|
| FDA product code | OUG |
| Device type | Medical Device Data System |
| Device class | Class 1 |
| Regulation | 21 CFR 880.6310 |
| Establishment | Specification developer, Complaint-file establishment, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2023-09-18 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Over the counter | Yes |
| Label carries | serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| MMT-7306 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Responder | Rauland-Borg Corporation | 170 |
| Medical Device Data System | Pentax of America, Inc. | 72 |
| DreamStation | Respironics Inc. | 55 |
| Endopro IQ | Pentax of America, Inc. | 49 |
| MonitAir | Monitair, LLC | 22 |
| Medical Device Data System | Medtronic, Inc. | 20 |
| DreamMapper | Respironics Inc. | 16 |
| Arthrex® | Arthrex, Inc. | 14 |
| Visionflex | Visionflex PTY Limited | 11 |
| Intesys Clinical Suite | Spacelabs Healthcare (Washington), Inc | 11 |
| myoncare | Oncare GmbH | 9 |
| MicroScan | Beckman Coulter, Inc. | 9 |
Showing 12 of 281. All products under Medical Device Data System
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2016-02-19 | Class II | Employee error | Medtronic MiniMed is recalling 19 CareLink iPro Therapy Management reports because the CareLink iPro reports were created using the Pacific Standard Time zone as the time reference, although the patients and their sensor data were subject t | 20 | 2016-05-16 |
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.