Company Quality Policy
BMG has been aiming at higher level quality management in accordance with global standards. In March 2007, BMG obtained ISO 13485 typically given to medical device companies satisfying global standard requirements. In 2022, BMG went through its 5th renewal.
| Applied Standard | JIS Q 13485:2018(ISO 13485:2016) |
| Certificate No. | JMAQA-M045 |
| Date | December 21, 2021 |
| Holder of Certificate | BMG Incorporated, Kyoto, JAPAN |
| Scope of Certificate | (a) Design, development, manufacture and distribution of surgical adhesives (absorbable tissue reinforcement), (b) Design, development, manufacture and distribution of surgical adhesives (absorbable tissue reinforcement) applicators, (c) Medical adhesives Design, development, manufacturing and distribution of raw materials |
| Certified by | Japan Management Association Examination and Registration Center |
| Applied Standard | EN ISO 13485：2016 (ISO 13485:2016)/DIN EN ISO 13485：2016 |
| Certificate No. | Q5 060103 0008 Rev. 02 |
| Date | March 5, 2007 |
| Holder of Certificate | BMG Incorporated, Kyoto, JAPAN |
| Scope of Certificate | Design and Development, Production and Distribution of Thermoplastic Denture Resin. The provision of Raw Materials for Medical Devices (Bio-absorbable Suture, Bone Fixation Material and Membrane Sheet for Periodontal Disease). |
| Certified by | TÜV SÜD Product Service GmbH |
BMG Inc.
〒601-8023
45 Minamimatsunoki-cho, Higashikujo, Minami-ku, Kyoto 601−8023, JAPAN
+81-75-681-0787
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