The PERIPROBE ANA-BFT anal probe is designed for perineal reeducation through manometric biofeedback. Its specific shape allows for accurate manometric recording, perfectly adapting to the anal morphology. There is no need to pre-inflate the balloon; simply connect the probe to the device before use. Avoid exposure to air and sunlight to prevent latex rubber aging. Compatible with devices equipped with standard Luer-lock pneumatic connections (ISO 594).

Position of use:
- Suitable for therapy on a bed

Technical features:
- Materials in contact with the patient: ABS + Rubber latex
- Invasiveness: anal orifice for a maximum period of 1 hour
- Dimensions: min/max diameter 8/12 mm, Length 100 mm
- Weight: 15 g
- Available colors: White
- Packaging: Supplied in single packaging (non-sterile) with warranty label and instructions for use
- Cleaning and disinfection: with water and neutral soap. Disinfect with alcohol and rinse with water before use. DO NOT sterilize.
- Personal use: It can be used for 60 sessions by a single patient
- Combined use: It must be used with an electromedical device (with CE marking) for manometric biofeedback and luer-lock pressure input (ISO 594) capable of detecting pressures from 0 to 300 cmH2O
- Production quality control: In ISO9001-ISO13485 certified system

Contraindications:
- Anal infections
- Do not use on people allergic to rubber latex

Usage and storage environment:
- From +5°C to +35°C with RH between 20% and 80%

CE marking:
- Class IIa device according to rule 5 Annex IX 93/42/EEC - CE0051 marking, issued by IMQ, according to Annex II of Directive 93/42/EEC
- Registration in the Medical Devices Registry of the Ministry of Health

CND:
- U070399

BD/RDM:
- 787075

• Materials in contact with the patient: ABS + Rubber latex.
• Invasiveness: anal orifice for a maximum period of 1 hour.
• Dimensions: ∅ min/max. 8/12 mm, Length 100 mm.
• Weight: 15 g.
• Available colors: White.
• Packaging: Supplied in single packaging (non-sterile) with warranty label and instructions for use.
• Cleaning and disinfection: with water and, if necessary, neutral soap. Disinfect with alcohol if necessary and rinse with water before use. DO NOT sterilize.
• Personal use: It can be used for 60 sessions by a single patient (it cannot be used by multiple patients)
• Combined use: It must be used with an electromedical device (with CE marking) for manometric biofeedback and luer-lock pressure input (ISO 594) capable of detecting pressures from 0 to 300 cmH2O.
• Production quality control: In ISO9001-ISO13485 certified system.

CONTRAINDICATIONS - Anal infections, - Do not use on subjects allergic to rubber latex.

Usage and storage environment: +5°C to +35°C with RH between 20% and 80%.
CE marking: Class IIa device according to rule 5 Annex IX 93/42/EEC - CE0051 marking, issued by IMQ, according to Annex II of Directive 93/42/EEC.
Registration in the Medical Devices Registry of the Ministry of Health

CND: U070399
BD/RDM : 787075
Ean :