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Fast-Pack pro - Indonesia BPOM Medical Device Registration

Fast-Pack pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603320688. The device is manufactured by CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is REVO MEDIKA PARAHYANGAN.

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 : B
Fast-Pack pro
Analysis ID: AKL 20603320688

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

REVO MEDIKA PARAHYANGAN

AR Address

Jl. Batununggal Indah II Ruko Blok RD 17 RT.01/RW.05, Desa/Kelurahan Mengger, Kec. Bandung Kidul, Kota Bandung, Provinsi Jawa Barat, Kode Pos: 40267

Registration Date

Sep 12, 2023

Expiry Date

Nov 03, 2027

Product Type

Surgical Dental Equipment

Dental handpiece and accessories

Non Radiation Electromedics

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