DR. HONLE DERMALIGHT 1000 - Indonesia BPOM Medical Device Registration
DR. HONLE DERMALIGHT 1000 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603716344. The device is manufactured by DR. K. HONLE MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DR. K. HONLE MEDIZINTECHNIK GMBH.Country of Origin
Germany
Authorized Representative
HERCA CIPTA DERMAL PERDANAAR Address
Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460
Registration Date
Jun 21, 2023
Expiry Date
Feb 15, 2028
Product Type
Surgical Equipment
Ultraviolet lamp for dermatologic disorders.
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