MATTES Caesarean Section - Indonesia BPOM Medical Device Registration
MATTES Caesarean Section is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103220245. The device is manufactured by MATTES INSTRUMENTE GMBH MEDIZINTECHNIK from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ARTHA MEDIKA SENTOSA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MATTES INSTRUMENTE GMBH MEDIZINTECHNIKCountry of Origin
Germany
Authorized Representative
PT. ARTHA MEDIKA SENTOSAAR Address
Ruko Rose Garden 5 Nomor 115, Grand Galxy City, Desa/Kelurahan Jakasetia, Kec. Bekasi Selatan, Kota Bekasi, Provinsi Jawa Barat, Kode Pos: 17147
Registration Date
Aug 29, 2022
Expiry Date
Mar 30, 2027
Product Type
Surgical Obstetric and Gynaecological Equipment
Obstetric-gynecologic general manual instrument.
Non Electromedic Non Sterile
MATTES Delivery Set
MATTES Episiotomy & Laceration Set
MATTES Embriotomy Set
MATTES Diagnostic Set
MATTES Polypectomy Set
MATTES Partus Set
MATTES Major Surgery Set
MATTES Hypophysectomy Set
MATTES Emergency Set
MATTES Basic Plastic Surgery Set
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