Fizza Surgical lists the Hank Uterine Dilator, Double Ended under 8 catalogue references, GY 12-355-01 to GY 12-355-08. Uterine dilators widen the cervical canal in graduated steps.
Catalogue references
| Reference | Description |
|---|---|
| GY 12-355-01 | Uterine Hank Double Ended 4.5 / 5.0mm Uterine dilators and depressors (5 mm) |
| GY 12-355-02 | Uterine Hank Double Ended 5.5 / 6.0mm Uterine dilators and depressors (6 mm) |
| GY 12-355-03 | Uterine Hank Double Ended 6.5 / 7.0mm Uterine dilators and depressors (7 mm) |
| GY 12-355-04 | Uterine Hank Double Ended 7.5 / 8.0mm Uterine dilators and depressors (8 mm) |
| GY 12-355-05 | Uterine Hank Double Ended 8.5 / 9.0mm Uterine dilators and depressors (9 mm) |
| GY 12-355-06 | Uterine Hank Double Ended 9.5 / 10.0mm Uterine dilators and depressors (10 mm) |
| GY 12-355-07 | Uterine Hank 6 Pieces per set, Double Ended, 4.5 / 5mm – 9.5 / 10mm Uterine dilators and depressors |
| GY 12-355-08 | Hank 6 Pieces per set, in canvas roll, 4.5 / 5mm – 9.5 / 10mm Uterine dilators and depressors |
Quote the reference you need when you send an inquiry.
Specification
| Material | AISI 304 / AISI 316 austenitic surgical-grade stainless steel |
| Sterilization | Steam autoclave to 134 °C · EtO compatible |
| Quality system | ISO 13485:2016 · CE-marked under EU MDR 2017/745 · FDA establishment-registered |
See the rest of the range under Uterine Dilators, Sound.
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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