ERMIS Tubectomy Set - Indonesia BPOM Medical Device Registration
ERMIS Tubectomy Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103123379. The device is manufactured by ERMIS MEDTECH GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DYRSA INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ERMIS MEDTECH GMBHCountry of Origin
Germany
Authorized Representative
PT. DYRSA INTERNATIONALAR Address
JL. SUKARAJA II NO. 277A RT.01 RW. 06 SUKARAJA CICENDO, BANDUNG
Registration Date
Jun 10, 2021
Expiry Date
May 11, 2025
Product Type
Surgical Obstetric and Gynaecological Equipment
Obstetric-gynecologic general manual instrument.
Non Electromedic Non Sterile
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