WOODPECKER - Plugger Fi-N - Indonesia BPOM Medical Device Registration
WOODPECKER - Plugger Fi-N is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603320600. The device is manufactured by GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is COBRA DENTAL INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD.Country of Origin
China
Authorized Representative
COBRA DENTAL INDONESIAAR Address
Jl. Pakuningratan No. 69
Registration Date
May 23, 2023
Expiry Date
Feb 23, 2027
Product Type
Surgical Dental Equipment
Dental hand instrument
Non Electromedic Non Sterile
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