Macintosh Fiber Optic Set of Five Blades — Catalogue reference DI-205-30.
- Macintosh fiber-optic blade with REMOVABLE light conductor (tool-free)
- Integrated fiber optic for best possible illumination
- 4 mm fiber-optic light conductor — up to 6,500 micro-fibers
- Compatible with all standard Fiber Optic handles
- AISI 303 / AISI 304 stainless steel with satin finish
- Smooth shape avoids sharp edges
- Fully autoclavable
- ISO 7376 standard fitting
| Reference / SKU | DI-205-30 |
| Pattern | Macintosh — fixed curved blade, removable light conductor |
| Light system | 4 mm Fiber Optic · 6,500 micro-fibers |
| Handle compatibility | Fiber Optic · ISO 7376 standard |
| Power supply | 2 × C-size batteries (standard) · 2 × AA-size (paediatric/stubby) |
| Material | AISI 303 / AISI 304 stainless steel (AISI 316 on fiber-optic variants) |
| Sterilization | Steam autoclave to 134 °C · EtO compatible |
| Quality system | ISO 13485:2016 · CE-marked under EU MDR 2017/745 · FDA establishment-registered |
The laryngoscope blade and handle are the airway clinician’s primary intubation tools. Two blade families dominate: the Macintosh (curved, indirect epiglottis elevation) and the Miller (straight, direct epiglottis lift). Size 0 covers neonatal intubation; sizes 1 and 2 paediatric; sizes 3 and 4 adult. Conventional bulb-illumination blades remain in use in some settings; fiber-optic blades have largely replaced them in operating theatres for the brighter, glare-free light at the tip. Handles come in small (paediatric) and large (adult) variants and must mate with the chosen blade family. Manufacturing demands tight tolerance on the blade hinge and the bulb/fiber connection. Fizza supplies complete intubation sets in stainless steel with optional fiber-optic upgrades.
Manufacturing compliance is verified through ISO 13485:2016 certification (the international medical-device quality standard), CE marking under EU MDR 2017/745, and FDA establishment registration. Certificate copies and regulatory documentation are available on request for inclusion in hospital procurement files and EU technical documentation packages. Sterilization validation follows ISO 17665 for steam autoclave at 134 °C.
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