EYETEC PVA SPONGE - Indonesia BPOM Medical Device Registration
EYETEC PVA SPONGE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203120726. The device is manufactured by NETWORK MEDICAL PRODUCTS LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KATAMATA OPTOMEDIK.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NETWORK MEDICAL PRODUCTS LTD.Country of Origin
United Kingdom
Authorized Representative
PT. KATAMATA OPTOMEDIKAR Address
Komplek Ketapang Indah Blok B2 No.31 Jl. KH. Zainul Arifin Kel.Krukut, Kec.Taman Sari Jakarta Barat
Registration Date
Dec 30, 2024
Expiry Date
Jul 26, 2029
Product Type
Surgical Eye Equipment
Ophthalmic sponge.
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