Catalogue number MAJ-2029, listed by Olympus Medical Systems Corp., Japan, under System, Imaging, Gastrointestinal, Wireless, Capsule. 1 manufacturer in China is registered for this product code.
Who Else Makes It
Registered in Hubei. One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Endocapsule Recorder SET | Listed by | Olympus Medical Systems Corp., Japan |
| FDA product code | NEZ |
| Device type | System, Imaging, Gastrointestinal, Wireless, Capsule |
| Device class | Class 2 |
| Regulation | 21 CFR 876.1300 |
| Establishment | Specification developer, Manufacturer, Exporter |
| Record published | 2016-09-21 |
| Record revised | 2025-11-24 (version 9) |
Specifications
Specifications | MRI safety | MR Unsafe |
| Prescription | Prescription only |
| Label carries | manufacturing date, serial number |
| Distribution end date | 2024-07-09 |
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.