Data / Medical devices / Ventilator, Non-Continuous (Respirator) / Malaysia
FDA-registered makers of Ventilator, Non-Continuous (Respirator) in Malaysia: 5 establishments
5 establishments in Malaysia are registered with the FDA to make Ventilator, Non-Continuous (Respirator) (product code BZD). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Ventilator, Non-Continuous (Respirator)
- Product code
- BZD
- Country
- Malaysia
Makers of Ventilator, Non-Continuous (Respirator) in Malaysia
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Mehow Medical (M) Sdn. Bhd. | Simpang Ampat Pulau Pinang, Malaysia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Meiban Micro Sdn Bhd | Ulu Tiram Johor, Malaysia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PPC Moulding Services (Malaysia) Sdn Bhd. | Senai Johor, Malaysia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rmo | Johor Bahru, Malaysia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ResMed Malaysia Operations Sdn Bhd | Senai Johor, Malaysia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.