CONMED Reflex Extractor - Indonesia BPOM Medical Device Registration
CONMED Reflex Extractor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603817387. The device is manufactured by CONMED CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HOSPI MEDIK INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CONMED CORPORATION.Country of Origin
United States
Authorized Representative
PT. HOSPI MEDIK INDONESIAAR Address
Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520
Registration Date
Jan 03, 2024
Expiry Date
Dec 31, 2026
Product Type
Surgical Equipment
Removable skin staple.
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