The Miller fiber optic laryngoscope blade is the straight blade that lifts the epiglottis directly, which is why it is often chosen for neonates, infants and difficult airways. Fizza Surgical makes it in six sizes, 00 to 4, under catalogue references DI-210-01 to DI-210-06. The light conductor is removable without tools and the blade fits fiber optic handles with the ISO 7376 fitting.
Sizes and catalogue references
| Blade size | Reference | Typical patient group |
|---|---|---|
| 00 | DI-210-01 | Premature neonates in NICU settings |
| 0 | DI-210-02 | Term neonates |
| 1 | DI-210-03 | Infants up to 12 months |
| 2 | DI-210-04 | Children and small adults, including difficult airways |
| 3 | DI-210-05 | Adults with difficult or anterior airways |
| 4 | DI-210-06 | Large adults with difficult airways |
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
- Miller straight 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
Specification
| Pattern | Miller — straight blade, removable light conductor |
| Light system | 4 mm Fiber Optic · 6,500 micro-fibers |
| 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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