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WOODPECKER Dental Anesthesia Device - Indonesia BPOM Medical Device Registration

WOODPECKER Dental Anesthesia Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605320702. 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 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 Dental Anesthesia Device
Analysis ID: AKL 20605320702

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

COBRA DENTAL INDONESIA

AR Address

Jl. Pakuningratan No. 69

Registration Date

Jul 28, 2023

Expiry Date

Feb 23, 2027

Product Type

Other Dental Equipment

Cartridge syringe.

Non Radiation Electromedics

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