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ORICARE A9800 Anesthesia Workstation - Indonesia BPOM Medical Device Registration

ORICARE A9800 Anesthesia Workstation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220338. The device is manufactured by ANY INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BETA MEDICAL.

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
ORICARE A9800 Anesthesia Workstation
Analysis ID: AKL 20403220338

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ANY INC.

Country of Origin

United States

Authorized Representative

PT. BETA MEDICAL

AR Address

Jl. Pangeran Antasari No. 212

Registration Date

Sep 02, 2023

Expiry Date

Sep 20, 2026

Product Type

Therapeutic Anesthesia Equipment

Gas machine for anesthesia or analgesia.

Non Radiation Electromedics

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