AGAPPE Mispa Plus - Indonesia BPOM Medical Device Registration
AGAPPE Mispa Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102320641. The device is manufactured by AGAPPE DIAGNOSTICS LTD. from India, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MULTIMEDILAB KARYAMANDIRI.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
AGAPPE DIAGNOSTICS LTD.Country of Origin
India
Authorized Representative
PT. MULTIMEDILAB KARYAMANDIRIAR Address
GP plaza lantai 3 unit 6, jalan Gelora II No. 01
Registration Date
Sep 20, 2023
Expiry Date
Mar 03, 2028
Product Type
Clinical Laboratory Equipment
Colorimeter, photometer, or spectrophotometer for clinical use.
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