Macintosh Fiber Optic Blade 00 (Ref DI-205-01) — Catalogue reference DI-205-01.
- 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-205-01 |
| 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.
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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