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EXIME®

Temporary Prostatic Stent

An innovative solution for acute or chronic urinary retention in males

EASY TO INSERT

FOR ALL PROSTATES

EXCELLENT TOLERANCE

EASY TO REMOVE

EXIME® COMPOSITION

EXIME® INDICATIONS FOR USE

EXIME® is intended for temporary use (up to 1 month) to restore urine flow and allow voluntary urination in males with acute or chronic urinary retention.

Efficient

Temporary ✓
Immediate voiding ✓
Increased Flow Rate ✓
Reduced PVR* ✓

SAFE

Does not require anesthesia ✓
Reduced Risk of CAUTI** ✓
Reduced Risk of MR bacteria selection ✓

EASY TO USE

Outpatient bedside procedure ✓
Sexual activity preservation ✓
No bladder spasms ✓

PATIENT COMFORT

Outpatient bedside procedure ✓
Sexual activity preservation ✓
No bladder spasms ✓

EXIME® HANDLING PROCEDURES

STEP 1

Before insertion of Exime

• Stretch the penis vertically.

• Instill the urethra with an anesthetic gel and calibrate with the 22 or 24 CH Bougie.

• Glide the Bougie until abutment against the posterior wall of the bulbous urethra.

• Note the depth of abutment of the Bougie.

STEP 2

Stent insertion

• Stretch the penis vertically again.

• Glide the device inside the urethra until abutment of the pusher tube against the posterior wall of the bulbous urethra.

STEP 3

Stent release

• Keep the penis stretched vertically.

• Remove the stylet and the pusher tube.

• Pull gently on the suture to feel the resistance of the wings of the upper tube deployed above the sphincter.

• Cut the retrieval suture: leave 3 mm protruding outside the meatus.

STEP 4

Control

• No urine leak when patient moves from the dorsal decubitus position to the standing position.

• Immediate micturition of clear urine.

STEP 5

Stent removal

• Instill the urethra with an anesthetic gel and calibrate the urethra meatus with a 22 or 24 CH Bougie.

• Pull gently on the suture with a forceps.

EXIME® KIT COMPOSITION

EXIME® TECHNICAL SPECIFICATIONS

EXIME®

Product CodeDescriptionKit componentsØ Size (Fr)Length (mm)
ROFV2200STEXIME®-M - Temporary
Prostatic Stent		Stent20 Prostatic part: 80 mm
Bulbar part: 32 mm
Pusher tube20 300
Flattener tube22 90
Bougies x222 & 24 300

Contraindications :
• Infection of the genito-urinary system, macroscopic haematuria with clots, sphincter insufficiency.
• Urinary tract diseases, such as urethral stenosis, urethral false route, bladder stones or other significant diseases that may affect the normal functioning of the device.

• Do not use after treatment with a physical agent generating prostatic oedema and possibly macroscopic haematuria (such as, hypo-fractionated radiotherapy, brachytherapy, focused ultrasound, trans-urethral micro- wave thermotherapy…), until the urine becomes clear (48h minimum).

• Do not use, when, on the advice of the doctor, such a procedure would be contrary to the greater interest of the patient.

This medical device is a regulated health product that bears, according to the regulations in force, the CE mark.
Products label and product instructions for Use (IFU) should be consulted before use of any product.
Product Risk Classification : IIa

EXIME IS NOT FDA CLEARED

   Instruction for use    Flyer
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Last updated on 2022-06-13