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PLANMECA ProScanner 2.0 - Indonesia BPOM Medical Device Registration

PLANMECA ProScanner 2.0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602126745. The device is manufactured by DรœRR DENTAL SE from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SATYA ABADI VISIMED.

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BPOM Registered
Risk Class Kelas Resiko : B
PLANMECA ProScanner 2.0
Analysis ID: AKL 20602126745

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DรœRR DENTAL SE

Country of Origin

Germany

Authorized Representative

PT. SATYA ABADI VISIMED

AR Address

Ruko Sentra Menteng Blok MN-28 Bintaro Jaya Sektor 7 Pondok Jaya Pondok Aren Tangerang 15224

Registration Date

Oct 03, 2022

Expiry Date

Mar 31, 2025

Product Type

Prosthetic Dental Equipment

Optical Impression Systems for CAD/CAM.

Non Radiation Electromedics

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