The Macintosh Mega fiber optic laryngoscope blade is the curved Macintosh pattern fitted with the larger 4 × 6 mm Mega Light fiber bundle, which puts more light at the blade tip than the standard 4 mm conductor. Fizza Surgical makes it in seven sizes, 00 to 5, under catalogue references DI-200-01 to DI-200-07, for fiber optic handles with the ISO 7376 fitting.
Sizes and catalogue references
| Blade size | Reference | Typical patient group |
|---|---|---|
| 00 | DI-200-01 | Premature neonates |
| 0 | DI-200-02 | Term neonates and small infants |
| 1 | DI-200-03 | Infants up to 12 months |
| 2 | DI-200-04 | Children 1–10 years |
| 3 | DI-200-05 | Most adult intubations |
| 4 | DI-200-06 | Large adults and bariatric patients |
| 5 | DI-200-07 | Extra-large adults and specialty cases |
Quote the reference for the size you need when you send an inquiry. The same blades are also supplied as sets of three, four or five blades.
Catalogue features
- Macintosh Mega Light fiber-optic blade — fixed curved geometry
- Outstanding light intensity via integrated fiber optics
- 4 × 6 mm Mega Light — 6,500 individual micro-fibers
- Compatible with all standard Fiber Optic handles
- AISI 303 / AISI 304 stainless steel with satin finish
- Smooth shape avoids sharp edges and cavities (easy to clean and sterilize)
- Fully autoclavable
- ISO 7376 standard handle fitting
Specification
| Pattern | Macintosh — fixed curved blade |
| Light system | 4 × 6 mm Mega Light · 6,500 micro-fibers (integrated FO) |
| Handle compatibility | Fiber Optic · ISO 7376 standard |
| 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 |
Handles and care
These blades are used with our fiber optic laryngoscope handles. For reprocessing see the laryngoscope sterilization protocol.
Made at the Fizza Surgical International facility in Sialkot, in operation since 1980, under ISO 13485:2016 with CE marking under EU MDR 2017/745 and FDA establishment registration.
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