Pocket otoscope Fiber optic — Pocket Otoscope Fiber Optic. Catalogue reference DI-500-20.
- Pocket form factor for daily clinical examination
- Fiber optic illumination through high-grade bundle
- Bayonet connecting system
- Chrome-plated knurled battery handle
| Reference / SKU | DI-500-20 |
| Light source | Fiber optic · 2.5V |
| Magnification | 3× lens |
| Power supply | 2 × C batteries (not included) |
| Packing | Soft pouch · with 4 reusable specula (2.5mm, 3.5mm, 4.5mm) |
| Material | AISI 304 / AISI 316 austenitic surgical-grade stainless steel |
| Sterilization | Steam autoclave to 134 °C · EtO compatible |
| Quality system | ISO 13485:2016 · CE-marked under EU MDR 2017/745 · FDA establishment-registered |
Diagnostic instruments cover the examination tools used in clinic settings: stethoscopes, otoscopes, ophthalmoscopes, percussion hammers, tuning forks, tongue depressors, and specialty examination patterns for specific anatomy (nasal specula, ear specula, vaginal specula). The diagnostic category sits between consumables and durable equipment — the patterns are reusable, autoclavable where applicable, and built to outlast many years of clinical use. Material requirements vary: examination instruments in contact with mucosa (specula, sound dilators, tongue depressors) use AISI 304 or AISI 316 austenitic stainless for corrosion resistance and biocompatibility; reflex hammers and tuning forks use bronze or specialty alloys for the acoustic and mechanical properties required. Fizza supplies the full diagnostic instrument range under ISO 13485:2016.
Fizza Surgical International has manufactured surgical instruments at its Sialkot, Pakistan facility since 1980 — more than four decades of continuous operation under one family ownership. The factory holds ISO 13485:2016 certification for medical devices and CE marking under EU MDR 2017/745, the regulatory baseline European hospitals and distributors require. FDA establishment registration covers exports to the United States.





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