ZONDA NEO Ventilator - Indonesia BPOM Medical Device Registration
ZONDA NEO Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403614713. The device is manufactured by TECME CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is CIPTA VARIA KHARISMA UTAMA.
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
Manufacturer
TECME CORPORATION.Country of Origin
United States
Authorized Representative
CIPTA VARIA KHARISMA UTAMAAR Address
Jl. Utan Kayu Raya No. 105A Jakarta
Registration Date
Sep 19, 2024
Expiry Date
Dec 31, 2028
Product Type
Therapeutic Anesthesia Equipment
Continuous ventilator.
Non Radiation Electromedics
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