DynaMesh-ENDOLAP 3D

Varying Pore Size The pore size of the device varies laterally to the longitudinal marking.

 

Product Range When selecting and cutting the device, sufficient defect overlap must be ensured to minimise the likelihood of the hernia recurring.

DynaMesh®-ENDOLAP 3D	09 cm x 14 cm	PV130914F1/F3
DynaMesh®-ENDOLAP 3D	10 cm x 15 cm regular	PV131015F1/F3
DynaMesh®-ENDOLAP 3D	12 cm x 17 cm	PV131217F1/F5
DynaMesh®-ENDOLAP 3D visible	09 cm x 14 cm	PV120914F1/F3
DynaMesh®-ENDOLAP 3D visible	10 cm x 15 cm	PV121015F1/F3
DynaMesh®-ENDOLAP 3D visible	12 cm x 17 cm	PV121217F1
	FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)

Can be used both for the right and the left side.

Features

Product	DynaMesh®-ENDOLAP 3D (1) DynaMesh®-ENDOLAP 3D visible (2)
Surgical Treatment	Inguinal Hernias / Femoral Hernias
Surgical Approach	Laparoscopic / Endoscopic
Surgical Technique	TAPP / TEP
Mesh Position	Preperitoneal (Posterior)
Fixation	(None)* / Sutures / Tissue Adhesives / Tacks
Green Central and Edge Marking
Visible Technology	(1) /  (2)
Materials	– Polyvinylidene fluoride (PVDF) (CAS 24937-79-9) > 99% (w/w) (1) (2) – Phthalocyanine green (CAS 1328-53-6) < 1% (w/w) (1) (2) – Triiron tetraoxide (CAS 1317-61-9) < 1% (w/w) (2)
Polymer (Monofilament)	PVDF
Biocompatibility	[TR1]
Ageing Resistance	[2A, 5VIT, 27A, 52VIT, 93A, 101]
Tear Propagation Resistance	[TR21]
Effective Porosity	High effective porosity reduces inflammation and the risk of excessive scar formation. [103P, TR23]
Klinge’s Mesh Classification	Class 1a [102P, TR23]
	* Based on current knowledge, with the exception of large direct inguinal hernias (European Hernia Society classification: M3), it appears possible to dispense with any form of fixation.

	Applies to all product sizes
	Does not apply
[#]	Reference “#”(see “References”)
[TR#]	Internal test report (see “internal test report references”)
Limitations	“A” animal trial, “B” bench test, “VIT” in-vitro trial, “P” published results based on the analysis of human mesh explants, “PB” published results mainly based on bench tests

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• Made of medical grade Silicone, have good biocompatibility, non-toxic.
• Exclusive soft seal cuff can be insert comfortable, minimizing potential trauma and increasing sealing.
• Strengthen neck and tip eases insertion and prevents folds.
• Kink-free tube eliminates the risk of airway tube occlusion.
• Have different size, suitable for neonate, infant, child and adult.
• Different color cuff, different material cuff, with aperture bar or not.
• Reusable types must be cleaned and disinfected or sterilizated before use only 40 times.

• Can be set as required sterilization temperature, working tem. range:room tem.:+5~126 Degree.
• Can ge set as required sterilization time of heat preservation, setting range:1~99min.
• Having a low water to stop heating function.
• This product uses the high quality stainless steel SUS304. Having to work under normal conditions adequate safety strength.

• Max Load: 250KG(550lb) in movement
• Material: steel electrostatic spraying
• Function:Backrest tilting From 0°to 75° ±5°
• Hi-lo function
• Reverse:14°±1°
• Trendelenburg:12°±1°
• Handset
• Abdomen auto-extension decompression
• PU knee crutches
• Adjustable hand grip
• phenolic compact laminate (HPL) bed board
• #304 stainless steel dirty bowl
• Backrest angle indicator
• Bumper wheels
• Pedal remote control
• Back-up battery

• The Ambu Oval Silicone resuscitator has a special textured surface combined with the unique support strap to ensures that a comfortable and firm grip is guaranteed, allowing for effective ventilation over extended periods, without the problem of hand fatigue.
• The Ambu Oval Silicone Resuscitators is made out of a view parts that can be disassembled easily. The Ambu Oval Silicone Resuscitator can easy be cleaned and autoclaved (except the oxygen reservoir) at a temperature of 134° Celsius.
• The unique shape is small and easy to hold. The ergonomic, lightweight design of Ambu Oval Silicone Resuscitator is made for optimal user handling and support even during extended ventilations.
• The resuscitators are semi-transparent allowing for a visual check of the patient’s condition. A pressure limitation valve is optional for the adult version and has been included into the design of the pediatric versions to ensure the safety of the patient*.

* International guidelines recommend that all manual resuscitators for infant and pediatric patients should be equipped with a pressure limitation mechanism so the airway pressure does not exceed 45 cm H2O.