Pure Global

SAMMORA Lancet Device Gold - Indonesia BPOM Medical Device Registration

SAMMORA Lancet Device Gold is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603020320. The device is manufactured by HANSOL MEDICAL CO. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SINTHE UTAMA 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
SAMMORA Lancet Device Gold
Analysis ID: AKL 11603020320

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

HANSOL MEDICAL CO.

Country of Origin

Korea

Authorized Representative

PT. SINTHE UTAMA INDONESIA

AR Address

Jl. Semangat No. 73 B Rt.017/ Rw.011 Kelurahan Mangga Dua Selatan Kecamatan Sawah Besar

Registration Date

Jan 24, 2023

Expiry Date

Oct 14, 2027

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing