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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.

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BPOM Registered
Risk Class Kelas Resiko : C
ZONDA NEO Ventilator
Analysis ID: AKL 20403614713

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

TECME CORPORATION.

Country of Origin

United States

Authorized Representative

CIPTA VARIA KHARISMA UTAMA

AR 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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