ProduktModell

Form	Modell	Außendurchmesser (Fr)	Arbeitslänge (mm)	Empfehlenswerter Führungsdraht (Zoll)
S Form	MD-S-UD-0840	8	400	0.028,0.035,0.038
	MD-S-UD-1040	10	400	0.028,0.035,0.038
	MD-S-UD-1240	12	400	0.028,0.035,0.038
	MD-S-UD-1440	14	400	0.028,0.035,0.038
	MD-S-UD-1640	16	400	0.028,0.035,0.038
	MD-S-UD-1840	18	400	0.028,0.035,0.038
	MD-S-UD-2040	20	400	0.028,0.035,0.038
	MD-S-UD-2240	22	400	0.028,0.035,0.038
	MD-S-UD-2440	24	400	0.028,0.035,0.038
	MD-S-UD-2640	26	400	0.028,0.035,0.038
L Form	MD-L-UD-0660	6	600	0.028,0.035,0.038
	MD-L-UD-0860	8	600	0.028,0.035,0.038
	MD-L-UD-1060	10	600	0.028,0.035,0.038
	MD-L-UD-1260	12	600	0.028,0.035,0.038
	MD-L-UD-1460	14	600	0.028,0.035,0.038
	MD-L-UD-1660	16	600	0.028,0.035,0.038
	MD-L-UD-1860	18	600	0.028,0.035,0.038
	MD-L-UD-2060	20	600	0.028,0.035,0.038
	MD-L-UD-2260	22	600	0.028,0.035,0.038
	MD-L-UD-2460	24	600	0.028,0.035,0.038
	MD-L-UD-2660	26	600	0.028,0.035,0.038
S-förmiges Paket	MD-A-UD-0060	8-26	600	0.028,0.035,0.038
L-förmiges Paket	MD-B-UD-0040	8-26	400	0.028,0.035,0.038

Indikation

Medical urethral dilator is used for dilation of the ureter prior to ureteroscopy and/or stone manipulation.

Merkmale

1.Die Dilatatoren haben eine hydrophile Beschichtung, die Flüssigkeiten anzieht und an den Dilatator hält.

2. Dadurch entsteht eine- reibungsarme, rutschige Oberfläche, um die Platzierung des Dilatators zu erleichtern und das Trauma des Patienten zu verringern.

3.Konisches Ende mit hervorragender Elastizität und ausgezeichneter Zähigkeit.

Produktionsfähigkeit

Our Company has, in conformity with national quality system standard, 100,000 clean-room facility and high quality testing platform, to ensure the quality of each product in accordance with international quality standards.

Urologische Produktlinie

Ureterführungsdraht, Steinfangkörbchen, Steinfangspule, Ureterstent, Ureterzugangsschleuse, Urethraldilatator etc.

Vorsichtsmaßnahmen

This device is sterile and intended for single use. It must be destroyed after

Verwendung gemäß den institutionellen Richtlinien für biologisch gefährlichen medizinischen Abfall.

Lager

After packaging, the device shall be stored in an environment that has

relative Luftfeuchtigkeit weniger als 80 Prozent, Temperatur 10 Grad - 40 Grad.

Ablauf für Sterilisation

Drei Jahre nach Sterilisation

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