ST. REED PLUS Epidural Catheter - Indonesia BPOM Medical Device Registration
ST. REED PLUS Epidural Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420284. The device is manufactured by SEAWON MEDITECH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KIMERA FLUX INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SEAWON MEDITECH CO., LTD.Country of Origin
Korea
Authorized Representative
PT. KIMERA FLUX INDONESIAAR Address
Ruko Melati Vista V21/A2 Jl.Boulevard
Registration Date
Apr 07, 2024
Expiry Date
Jan 24, 2026
Product Type
Therapeutic Anesthesia Equipment
Anesthesia conduction catheter.
Non Electromedic Sterile

