HUDSON RCI SHERIDAN / SPIRAL FLEX - Indonesia BPOM Medical Device Registration
HUDSON RCI SHERIDAN / SPIRAL FLEX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403111241. The device is manufactured by HUDSON RESPIRATORY CARE TECATE S. DE R.L. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Country of Origin
Mexico
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Oct 27, 2021
Expiry Date
Dec 31, 2023
Product Type
Therapeutic Anesthesia Equipment
Tracheal tube.
Non Electromedic Sterile
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