Mahe Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Mahe Intl., Inc. makes
Mahe Intl., Inc. manufactures endoscopic instruments, including pediatric nasopharyngoscopes and their associated accessories. The portfolio also covers ancillary equipment and additional endoscopic tools designed for procedural use.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Mahe Instruments Ref K942823
Regimes: 510(k) Registry: 510(k)Mahe Pediatric Naso Pharyngoscope Its Associated And Ancillary Equipment And Endoscopic Accessories Ref K030857
Regimes: 510(k) Registry: 510(k)Mahe Instruments Ref K991426
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mahe Intl., Inc. have in the registry?
The registry currently lists 3 devices for Mahe Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mahe Intl., Inc.'s devices?
Among its 3 most recently registered devices, Mahe Intl., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Mahe Intl., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mahe Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mahe Intl., Inc. in the registry?
The most recently registered devices listed for Mahe Intl., Inc. include MAHE INSTRUMENTS and MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES.