McCoy Flexible Tip Mega Fiber Optic Blade 3 (Ref DI-100-03) — Catalogue reference DI-100-03.
- McCoy lever-controlled flexible tip — adjustable through 90° for difficult intubation
- Outstanding light intensity with LED illumination via extra-strong fiber bundle
- 4 × 6 mm Mega Light — 6,500 individual micro-fibers
- Reduced force required to visualize the larynx
- Reduced likelihood of damage to teeth and soft tissues
- AISI 303 / AISI 304 stainless steel with satin finish
- Fully autoclavable and easier to clean
- ISO 7376 standard handle fitting
| Reference / SKU | DI-100-03 |
| Size | Size 3 (adult medium) |
| Blade dimensions | 135 mm × 113 mm |
| Pattern | McCoy flexible-tip — Macintosh-derivative |
| Light system | 4 × 6 mm Mega Light · 6,500 micro-fibers |
| Handle compatibility | Fiber Optic · ISO 7376 standard |
| Power supply | 2 × C-size batteries (in compatible handle) |
| 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.
Reviews
There are no reviews yet.