FERNO Vacuum Splint - Indonesia BPOM Medical Device Registration
FERNO Vacuum Splint is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11602220038. The device is manufactured by FERNO-WASHINGTON, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MADESA SEJAHTERA UTAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FERNO-WASHINGTON, INC.Country of Origin
United States
Authorized Representative
MADESA SEJAHTERA UTAMAAR Address
JL. GUNUNG SAHARI RAYA 51- A NO.14
Registration Date
Aug 29, 2023
Expiry Date
Jul 05, 2025
Product Type
Prosthetic Surgical Equipment
Noninflatable extremity splint.
Non Electromedic Non Sterile
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