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EMS AIR-FLOW Handy 3.0 Mobile Prophylaxis Device - Indonesia BPOM Medical Device Registration

EMS AIR-FLOW Handy 3.0 Mobile Prophylaxis Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603220408. The device is manufactured by EMS ELECTRO MEDICAL SYSTEMS S.A. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FONDACO JAYATAMA.

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
EMS AIR-FLOW Handy 3.0 Mobile Prophylaxis Device
Analysis ID: AKL 20603220408

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

PT. FONDACO JAYATAMA

AR Address

Agung Podomoro Land Tower, Podomoro City Lt. 27 T1, T2, T5 Jl. Letnan Jendral Siswondo Parman Kav. 28 Kel. Tanjung Duren Selatan, Kec. Grogol Petamburan, Jakarta Barat, DKI Jakarta

Registration Date

Dec 13, 2022

Expiry Date

Mar 21, 2027

Product Type

Surgical Dental Equipment

Dental handpiece and accessories

Non Radiation Electromedics

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