OUR SERVICE
 We provide audit service for certification of the specially controlled medical devices provided by the Pharmaceutical and Medical Device Act (“PMD Act”).
We are officially registered in the Ministry of Health, Labor and Welfare as the Certification Body (Registration Number: AM).

CERTIFYING PRODUCTS
 We provide our services for the following products (Class II) under Section 1 of Article 23-2 -23 of PMD Act.

[ Items ]
 ・Anesthetic and respiratory equipment
 ・Dental devices
 ・Medical electrical equipment
 ・Facility equipment
 ・Non-active implantable equipment
 ・Ophthalmic and visual equipment
 ・Reusable equipment
 ・Single-use equipment
 ・Home use massager, home use electronical therapy equipment and related equipment
 ・Hearing aids
 ・Radiation and diagnostic imaging equipment
 *Active implantable equipment and in-vitro diagnostic reagents are not covered by us.

 

COMPANY NAME

   Fujipharma Corparation

ESTABLISHMENT DAY

   February 3 , 2004

CONTACT US

  Fujipharma Corparation

Address:
327-2 Nishikumando,
Numazu City,
Shizuoka Pref.,
410-0051, Japan
E-mail:
fujipharma@fujipharma.co.jp
TEL:
(+81) 055-955-8393
FAX:
(+81) 055-955-8285

 

[ Home ]