Pure Global

AMO i Design Advanced Wavescan Studio - Indonesia BPOM Medical Device Registration

AMO i Design Advanced Wavescan Studio is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201810722. The device is manufactured by AMO MANUFACTURING USA LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDIUM FIRST.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
AMO i Design Advanced Wavescan Studio
Analysis ID: AKL 11201810722

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. MEDIUM FIRST

AR Address

The Bellezza Permata Hijau GP Office Tower Lantai 27 No. 03, Jl. Letjen Soepeno No. 34, Jakarta

Registration Date

Nov 07, 2022

Expiry Date

Sep 08, 2027

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from AMO MANUFACTURING USA LLC.
Products from the same manufacturer (2 products)