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EDGEONE GLIDEPATH ™ EDGEENDO - Indonesia BPOM Medical Device Registration

EDGEONE GLIDEPATH ™ EDGEENDO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603320715. The device is manufactured by US ENDODONTICS, LLC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is THE LIGHT OF THE THREE ETERNAL STARS.

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BPOM Registered
Risk Class Kelas Resiko : A
EDGEONE GLIDEPATH ™ EDGEENDO
Analysis ID: AKL 10603320715

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

THE LIGHT OF THE THREE ETERNAL STARS

AR Address

Jl. Musi No. 8 RT 012/002, Cideng, Gambir

Registration Date

Sep 29, 2023

Expiry Date

Apr 17, 2028

Product Type

Surgical Dental Equipment

Dental hand instrument.

Non Electromedic Non Sterile

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