Proscope™
Chestpiece-660, 661,Adult, Silver
6manufacturers in China registered for this device type
4catalogue numbers in this listing
Who Else Makes It
Concentrated in Zhejiang (3), Jiangsu (2), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Hangzhou Rollmed Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 127 |
| Hospital & Homecare IMP. & EXP. Co., Ltd. | Nanjing | Jiangsu | Contract manufacturer | 179 |
| Danyang NEW Hope Medical Equipment Co., Ltd. | Danyang | Jiangsu | Manufacturer | 38 |
| ADC Ningbo Co., Ltd. | Ningbo | Zhejiang | Exporter | 13 |
| MDF Instruments Medifriend Inc. | Song Jiang District | Shanghai | Repacker / relabeller | 13 |
| Ningbo Jiangbei Tenso Medical Instruments Co., Ltd. | Ningbo | Zhejiang | Manufacturer | 4 |
Record
| Listed by | American Diagnostic Corp., United States |
|---|---|
| FDA product code | BZS |
| Device type | Stethoscope Head |
| Device class | Class 1 |
| Regulation | 21 CFR 868.1930 |
| Establishment | Contract manufacturer, Repacker / relabeller, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2016-09-27 |
| Record revised | 2024-11-25 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Over the counter | Yes |
| Label carries | lot or batch number |
| Packaging | Inner pack of 10 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 660-01 | In distribution | |
| 676-01 | In distribution | |
| 670-01 | In distribution | |
| 675-01 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Adscope® | American Diagnostic Corp. | 83 |
| AincA® | Anesthesia Associates, Inc. | 17 |
| SunMed | SunMed Group Holdings, LLC | 13 |
| Adimals® | American Diagnostic Corp. | 5 |
| Hopkins Medical Products® | Hopkins Uniform Company | 2 |
| Adscope® Vistascope™ | American Diagnostic Corp. | 1 |
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.