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PUREMED Blood Lancets - Indonesia BPOM Medical Device Registration

PUREMED Blood Lancets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603024897. The device is manufactured by HUAIAN HELEN MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ROYAL SEJAHTERA MANDIRI.

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 : A
PUREMED Blood Lancets
Analysis ID: AKL 11603024897

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. ROYAL SEJAHTERA MANDIRI

AR Address

Ruko Mahkota Ancol Blok E No.53, Jl. RE Martadinata, Kelurahan Pademanagn Barat

Registration Date

Mar 30, 2023

Expiry Date

Jul 13, 2025

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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