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WOODPECKER Ultrasonic Endo Activator Device - Indonesia BPOM Medical Device Registration

WOODPECKER Ultrasonic Endo Activator Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603127344. The device is manufactured by GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
WOODPECKER Ultrasonic Endo Activator Device
Analysis ID: AKL 20603127344

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. COBRA DENTAL INDONESIA

AR Address

Jl. Pakuningratan No. 69

Registration Date

Oct 21, 2022

Expiry Date

Feb 23, 2027

Product Type

Surgical Dental Equipment

Ultrasonic scaler.

Non Radiation Electromedics

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