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SAPPHIRE Z200NG - Indonesia BPOM Medical Device Registration

SAPPHIRE Z200NG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603221792. The device is manufactured by BERGER & KRAFT MEDICAL SP. Z O. O. from Poland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.

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
SAPPHIRE Z200NG

ZAFFIRO Z200NG

Analysis ID: AKL 21603221792

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Poland

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Sultan Iskandar Muda No. 7A & B

Registration Date

Aug 16, 2022

Expiry Date

Sep 01, 2026

Product Type

Surgical Equipment

Laser surgical instrument for use in general and plastic surgery and in dermatology.

Non Electromedic Sterile

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