The straight working axis suits midline access and procedures where the surgeon’s line of sight aligns with the instrument shaft. The tungsten-carbide tip inserts resist wear under repeated needle-grip cycles, making this a premium choice for high-volume operating theatres. The Metzenbaum TC Dissecting Scissors — Straight Delicate, 18 cm (18.0 cm) ships under reference SC 02-817-03.
Myron Firth Metzenbaum’s name attaches to the long, slender dissecting scissors used across general, vascular, and thoracic surgery for blunt and sharp tissue dissection. Developed in 1920s Cleveland, Metzenbaum scissors differ from Mayo scissors in their thinner blade profile and longer shaft-to-blade ratio — roughly 2:1 versus Mayo’s 1:1 — making Metzenbaums ideal for deep tissue planes where Mayo’s heavier blade would be cumbersome. The 14 cm, 17 cm, 20 cm, and 23 cm lengths are standard. Curved blades dominate operating-theatre trays; straight Metzenbaums are reserved for specific cuts. Tungsten carbide tipped variants are the long-service option. Surgeons request Mayo for fascia and suture, Metzenbaum for delicate dissection.
| Reference / SKU | SC 02-817-03 |
| Pattern | Metzenbaum |
| Working length | 18 cm (180 mm) |
| Shape | Straight |
| Tip configuration | TC tips |
| Material | AISI 420 martensitic stainless steel (tungsten-carbide insert variants on TC SKUs) |
| Sterilization | Steam autoclave to 134 °C · EtO compatible |
| Quality system | ISO 13485:2016 · CE-marked under EU MDR 2017/745 · FDA establishment-registered |
- Metzenbaum TC Dissecting Scissors — Curved Standard, 18 cm (SC 02-816-03)
- Metzenbaum TC Dissecting Scissors — Curved Delicate, 18 cm (SC 02-827-03)
- Metzenbaum TC Dissecting Scissors — Straight Standard, 18 cm (SC 02-815-03)
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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