2 catalogue numbers from D30200-210, listed by Healthmark Industries Co., Inc., United States, under Bulb, Inflation, For Endoscope. 4 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Shanghai (2), Zhejiang (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Disposable Bulb & Bladder | Listed by | Healthmark Industries Co., Inc., United States |
| FDA product code | FCY |
| Device type | Bulb, Inflation, For Endoscope |
| Device class | Class 1 |
| Regulation | 21 CFR 876.1500 |
| Establishment | Specification developer, Repacker / relabeller, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2022-12-08 |
| Record revised | 2024-07-23 (version 4) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Storage | Storage environment temperature 2 to 25 °C |
| Distribution end date | 2024-02-23 |
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.