Pure Global

WOODPECKER - Dental Diode Laser Device - Indonesia BPOM Medical Device Registration

WOODPECKER - Dental Diode Laser Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420439. The device is manufactured by GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is COBRA DENTAL 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 : C
WOODPECKER - Dental Diode Laser Device
Analysis ID: AKL 21603420439

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

COBRA DENTAL INDONESIA

AR Address

Jl. Pakuningratan No. 69

Registration Date

Feb 22, 2024

Expiry Date

Feb 23, 2027

Product Type

Surgical Equipment

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

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing