Catalogue number CATW1A212BL, listed by Laborie Medical Technologies, Canada ULC, under Device, Cystometric, Hydraulic. 3 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Guangdong (2), Zhejiang (1). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Catheter, Pabd, Dual Lumen, Closed Balloon, Latex, 12Fr | Listed by | Laborie Medical Technologies, Canada ULC |
| FDA product code | FEN |
| Device type | Device, Cystometric, Hydraulic |
| Device class | Class 2 |
| Regulation | 21 CFR 876.1620 |
| Premarket notification | Exempt |
| Record published | 2017-11-01 |
| Record revised | 2018-03-29 (version 2) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Sterilisation | Ethylene Oxide |
| Supplied sterile | Yes |
| Single use | Yes |
| Latex | Contains natural rubber latex |
| Label carries | lot or batch number, expiry date, serial number |
| Packaging | Pack of 100, pack of 10 |
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.