Pure Global

GENERAL CARE Penlight SS - Indonesia BPOM Medical Device Registration

GENERAL CARE Penlight SS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903121405. The device is manufactured by WENZHOU YI HONG MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GRAHA MEGATAMA 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
GENERAL CARE Penlight SS
Analysis ID: AKL 10903121405

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. GRAHA MEGATAMA INDONESIA

AR Address

BIZ PARK 3 COMMERCIAL ESTATE BLOK E NOMOR 9, JALAN SULTAN AGUNG KM 28.5

Registration Date

Feb 12, 2024

Expiry Date

Feb 12, 2027

Product Type

General Hospital Equipment and Other Individuals

Battery-powered medical examination light.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing