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PERTHESE® SENSITIVE round, textured implants,
medium cohesivity:
BMX, BMP, B540 and B550

Medium cohesive Silicone Gel-filled Breast Implant

NEW!  Please ask for our documentation and presentation material for this product!

Tri-laminated Micro-Textured surface. Medium cohesive gel integrated with the shell for a Sensitive touch, slightly firmer than the Standeard Perthese implants.


 

SAFETY
  • The PERTHESE® breast implant is a sterile gel-filled implant made from a trilaminar silicone envelope. The silicone envelope consists of an internal and external layer made from a high mechanical resistance medical grade silicone elastomer and an intermediate barrier layer to significantly reduce gel bleed. The envelope is filled with a soft transparent silicone gel, very close to the normal breast consistency. The elongation of the shell is greater than 500%. These implants form an extremely soft and resilient structure, limiting gel migration to a minimum.
  • The PERTHESE® mammary implants are manufactured and packaged under the ISO9001/EN 46001 quality standards applicable to medical devices. Quality controls are performed at all stages of the production.
  • Each implant carries the manufacturer's identification, the serial number and the volume (in cc) engraved on the patch.
  • The PERTHESE® breast implants are provided sterile in a rigid double blister package in order to ensure security and convenience. The prosthesis is sterilized by ethylene oxide.
  • The base of PERTHESE® AX anatomic mammary implants has five positioning blocks helping to hand-position in the space.
 

PERTHESE® SENSITIVE BMX REFERENCE DATA

Moderate profile gel-filled textured breast implant


   References Volume cc Diameter Projection
  BMX 100
BMX 125
BMX 150
BMX 175
BMX 200
BMX 225
BMX 250
BMX 275
BMX 300
BMX 325
BMX 350
BMX 375
BMX 400
BMX 450
BMX 500
BMX 550
BMX 600
BMX 650
BMX 700
BMX 800		 100
125
150
175
200
225
250
275
300
325
350
375
400
450
500
550
600
650
700
800		 9,1
9,6
10,2
10,8
11,5
12,0
12,5
12,7
12,8
12,9
13,2
13,7
13,9
14,2
14,5
14,8
15,2
15,5
15,6
16,5		 2,7
3,0
3,1
3,2
3,3
3,4
3,5
3,8
4,0
4,2
4,3
4,4
4,8
4,9
5,0
5,5
5,6
5,8
6,2
6,3
 

PERTHESE® SENSITIVE BMP REFERENCE DATA

Moderate Plus profile gel-filled textured breast implant


   References Volume cc Diameter Projection
  BMP 115
BMP 135
BMP 165
BMP 190
BMP 225
BMP 260
BMP 305
BMP 320
BMP 345
BMP 380
BMP 410
BMP 440
BMP 475
BMP 510
BMP 580
BMP 635
BMP 685
BMP 735
BMP 800
BMP 910		 115
135
165
190
225
260
305
320
345
380
410
440
475
510
580
635
685
735
800
910		 8,9
9,4
10,2
10,7
11,3
11,8
12,3
12,6
12,8
13,0
13,4
13,5
13,8
14,2
14,5
14,8
15,2
15,5
15,6
16,5		 3,1
3,2
3,5
3,6
3,7
3,9
4,1
4,4
4,6
4,7
4,8
5,0
5,2
5,3
5,8
6,0
6,1
6,4
6,6
6,9
 

PERTHESE® SENSITIVE B540 REFERENCE DATA

High profile gel-filled textured breast implant


   References Volume cc Diameter Projection
  B540-090
B540-100
B540-130
B540-165
B540-195
B540-215
B540-245
B540-270
B540-280
B540-315
B540-335
B540-360
B540-390
B540-410
B540-455
B540-520
B540-550
B540-605
B540-650
B540-850		 90
100
130
165
195
215
245
270
280
315
335
360
390
410
455
520
550
605
650
850		 8,3
8,5
9,0
9,7
10,2
10,5
10,8
11,2
11,5
11,7
12,0
12,2
12,5
12,6
12,8
13,6
13,7
14,2
14,6
15,9		 2,8
3,1
3,4
3,8
4,0
4,3
4,5
4,6
4,7
4,9
5,0
5,1
5,2
5,4
5,6
5,8
6,0
6,2
6,4
6,9
 

PERTHESE® SENSITIVE B550 REFERENCE DATA

Ultra-high profile gel-filled textured breast implant


   References Volume cc Diameter Projection
  B550-095
B550-125
B550-150
B550-160
B550-175
B550-195
B550-215
B550-235
B550-265
B550-285
B550-315
B550-330
B550-345
B550-390
B550-410
B550-425
B550-445
B550-485
B550-530
B550-580
B550-630
B550-705		 95
125
150
160
175
195
215
235
265
285
315
330
345
390
410
425
445
485
530
580
630
705		 7,6
8,3
9,0
9,1
9,4
9,7
10,1
10,2
10,6
10,9
11,3
11,4
11,5
12,0
12,2
12,3
12,4
12,7
13,1
13,5
13,8
14,2
 3,4
3,7
3,8
4,1
4,2
4,2
4,4
4,5
4,7
4,9
5,0
5,2
5,3
5,3
5,6
5,7
5,8
5,9
6,1
6,3
6,5
6,9
 

* Measurements are obtained by placing the pre-filled unit on a concave shape surface.

Please note: individual implant dimensions may vary slightly in products of this type. Not all units will conform exactly to the above dimensions.
 

INDICATIONS – CONTRAINDICATIONS
  • Contour reconstruction and size augmentation following a subcutaneous mastectomy for benign disease as for example chronic cystic mastitis, or for augmentation or reconstruction for correction of defects following radical mastectomy procedures.
  • Unilateral or bilateral mammary augmentation or reconstruction to surgically correct various congenital or acquired anomalies such as amastia, aplasia, hypomastia, hypoplasia or for cosmetic purposes.

It is the surgeon’s sole responsibility to determine criteria for the patient selection

PERTHESE® mammary prostheses should not be implanted in patients with:

  • a general or localized infection of the mammary sphere.
  • a history of auto-immune disease
  • an ongoing pregnancy.
 

PRECAUTIONS FOR USE
Precautions for use should be considered by the surgeon prior to the use of a PERTHESE® mammary prosthesis:
  • No evaluating breast cancer at the time of implantation, even if a breast reconstruction can be considered in the case of a controlled metastatic syndrome, the prerequisite being to well balance the benefits to the patient with the consequences of the surgical procedure and its non-interference with the required carcinologic treatments.
  • If the patient exhibits a lack of skin it is the sole responsibility of the surgeon to decide the use of an expansion technique or a tissue graft.
  • Patient is not willing to accept the possibility of multiple surgeries for revision, which could be related to a lack of understanding, or inappropriate motivation, or to a history of repeated failures following cosmetic augmentations or subcutaneous mastectomy.
  • On a general point of view, the health condition of the patient should be considered in view of the type of surgical procedure and the required anesthesia. Each patient must be evaluated by the surgeon to balance the risk/benefit to the patient.
 
"The product quality" (PDF, 324 KB)
 
WARRANTY
Pérouse Plastie introduces a new Quality Insurance Program which includes:
  • In case of rupture of the implant, free replacement with an identical product during 15 years from the date of its implantation
  • In case of capsular contracture Baker III and IV in augmentation surgery, free replacement product with an identical product during a period of 10 years from the date of its date of implantation.

Please ask us for the full text and conditions of the warranty: info@hojmed.com

PEROUSE PLASTIE warrants that reasonable care in selection of materials and methods of manufacture were used in fabrication of these products.
PÉROUSE PLASTIE shall not be liable for any incidental or consequential loss, damage, or expense, directly or indirectly arising from the use of these products.

The foregoing warranties, as conditioned and limited, are in lieu of and exclude all other warranties not expressly set forth herein, whether express or implied by operation of law or otherwise.

PEROUSE PLASTIE neither assumes nor authorizes any other person to assume for it any other or additional liability or responsibility in connection with these products.
PEROUSE PLASTIE intends that these products should be used only by physicians having appropriate training in plastic and reconstructive surgery techniques.

PERTHESE® is a registered Trademark of PEROUSE PLASTIE. Made in France by PEROUSE PLASTIE.

© Höjmed AB – 2006

info@hojmed.com