WILLMEDIC urinary catheter according to TU 32.50.13-007-85403248-2025

Manufacturer: April Limited Liability Company

Legal address: 350042, Krasnodar Krai, Krasnodar, 40 Let Pobedy Street, 14/2, room 2

Place of production:
1) Hubei Handry Medical Appliance Co., Ltd.
(Hubei Hendry Medical Appliance Co., Ltd.)
Block 1, Building 2, Yinhu Science and Technology Park, Xiaohan Avenue, Xiaonan District, Xiaogan City, Hubei Province, China
(Unit 1 Building 2, Yinhu Science and Technology Park, Xiaohan Avenue, Xiaonan District, Xiaogan City, Hubei Province, China)
2) LLC "Aprel"
353254, Krasnodar Krai, Seversky Municipal District, Smolenskoye Rural Settlement, Stanitsa Smolenskaya, M. Gorkogo Street, 43 V

Phone: 8 861-212-32-82
E-mail: torgionline@gmail.com

SAFETY PRECAUTIONS

WARNING!
For external use only.
Use with caution if you have a history of skin allergies.
Do not apply directly to open or infected wounds, ulcers, or second-degree or greater burns.
If you have open wounds or ulcers in the stoma area, use with caution and only after consulting a specialist.
Avoid contact with the eyes and mucous membranes.
Close the lid tightly after each use to prevent the product from drying out or hardening.
Keep out of reach of children.

USED SYMBOLS

Name

WILLMEDIC urinary catheter according to TU32.50.13-007-85403248-2025

Purpose

The urinary catheter is used to drain urine from people who are unable to empty their urine naturally, and for intermittent (temporary) catheterization.
The product is sterile and single-use.
It is not subject to cleaning, sterilization, disinfection, maintenance, or repair.

APPEARANCE AND GENERAL DESCRIPTION OF THE DESIGN VARIANT

A catheter is a flexible tube consisting of a shaft, a drainage port with a channel connector.
The Nelaton standard catheter has a straight shaft with a blind end and an oval hole on the side.
The Timmann catheter has a shaft with a blind end in the form of a curved beak and an oval hole on the side.

INDICATIONS FOR USING THE IMPLEMENTATION OPTION

Chronic or acute urinary retention;
Incontinence or urinary incontinence;
Collection of a urine sample for analysis;
Measurement of residual urine volume and monitoring of urine output;
Urine removal in patients in a coma;
Urine removal in patients who are unable to empty their bladders on their own; patients who are under the influence of anesthetics or sedatives during the preoperative or rehabilitation period;
Postoperative rehabilitation of the genitourinary system.
The product is used under the prescription of a doctor. Depending on the indications, the catheterization is performed by a medical professional or by the patient themselves.

Contraindications

Acute infectious and inflammatory diseases of the male genitals and urethra;
Urethral strictures;
Urethral injuries;
Urethral fistula;
Priapism;
Reconstructive surgeries on the urethra or bladder;
Individual intolerance to materials.

SIDE EFFECTS

The following complications may occur during catheterization:
Injury to the urethra or bladder with bleeding or microhematuria;
Skin injuries;
Infection of the urinary tract;
Creation of false passages;
Scarring and formation of strictures;
Perforation of the bladder;
Paraphimosis.

SCOPE OF APPLICATION

Departments of urology, internal medicine, surgery, oncology, obstetrics and gynecology, and therapy; rehabilitation; at home and in medical and preventive institutions.

POTENTIAL CONSUMER

Patients; patients' relatives, care specialists, and medical staff.
Only a doctor performs the procedure on children.

METHOD OF APPLICATION:

Before use, consult your doctor to determine the type and size of the catheter, as well as the frequency of the procedure.
 Before the procedure, thoroughly cleanse the genital area.
The depth of insertion of the Nelaton catheter for intermittent catheterization corresponds to the length of the urethra: 4-6 cm for women and 18-20 cm for men. The catheter is inserted until urine appears.
To prepare the urethral catheters for insertion, use lubricants such as anesthetic and antiseptic gels. When using latex catheters, do not use petroleum-based lubricants.
Nelaton Catheter
Start by washing your hands to prevent bacterial contamination.
Clean and disinfect the urethral area using proper aseptic techniques before insertion.
Open the package, remove the catheter, and fully immerse it in sterile water. Leave the catheter for at least 30 seconds to fully activate the hydrophilic coating.
Use one hand to place the catheter tip in the urethra, and use the other hand to gently insert the

Pre-lubricated catheter
Start by washing your hands to prevent bacterial contamination.
Clean and disinfect the urethral area using the necessary aseptic technique before insertion.
Open the package and remove the catheter.
Place the catheter tip in the urethra with one hand, and use the other hand to gently insert the lubricated catheter into the urethra until urine begins to flow from the drainage port.
You can drain the urine directly into a toilet or a special container.
When the bladder is empty, slowly remove the catheter and dispose of it along with the packaging.
Attention! Do not use petroleum-based ointments or lubricants.

CONDITIONS OF TRANSPORTATION, STORAGE, AND OPERATION

The product should be protected from strong pressure, direct sunlight, rain, and snow.
Operating conditions:
– temperature: -10°C to +50°C
– humidity: 30-80%
Storage conditions:
Store in the manufacturer's packaging in a dry, dark, cool place that is out of reach of children.
– temperature: -10°C to +50°C
– humidity: 30-80%
Transportation conditions:
Transport by all types of vehicles in the manufacturer's packaging.
– temperature: -10°C – +50°C
– humidity: 30-80%

DISPOSAL OF A MEDICAL PRODUCT

At home:
after use, dispose of it with solid household waste.
In medical and preventive institutions:
Unused products and packaging are disposed of in accordance with local regulations as Class A waste.
When using medical products in infectious disease departments, used products are disposed of in accordance with local regulations as Class B waste.

Expiration date

Product shelf life: 5 years from the date of manufacture indicated on the packaging.
Do not use the product after the expiration date.

MANUFACTURER'S GUARANTEES

The manufacturer guarantees that the product meets the declared characteristics if the consumer follows the conditions of use, transportation, and storage.
The product is guaranteed to remain sterile for 5 years from the date of manufacture indicated on the packaging.

INFORMATION ABOUT COMPLAINTS

Claims are made in accordance with the established procedure at the manufacturer's address
APRIL LLC, Russia