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SERENITY Latex Examination Gloves (Powdered) - Indonesia BPOM Medical Device Registration

SERENITY Latex Examination Gloves (Powdered) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903121111. The device is manufactured by FITONE LATEX PRODUCTS CO., LTD., GUANGDONG from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SERENITY 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 : A
SERENITY Latex Examination Gloves (Powdered)
Analysis ID: AKL 10903121111

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SERENITY INDONESIA

AR Address

Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter

Registration Date

Mar 01, 2021

Expiry Date

Aug 20, 2025

Product Type

General Hospital Equipment and Other Individuals

Patient examination glove.

Non Electromedic Non Sterile

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