PAUL Glaucoma Implant - Indonesia BPOM Medical Device Registration
PAUL Glaucoma Implant is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21202220005. The device is manufactured by SUNNINGDALE TECH LTD. from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUNNINGDALE TECH LTD.Country of Origin
Singapore
Authorized Representative
PT. TRANSMEDIC INDONESIAAR Address
PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137
Registration Date
May 29, 2023
Expiry Date
Jan 08, 2028
Product Type
Prosthetic Eye Equipment
Aqueous shunt.
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