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3M ESPE monophase - Indonesia BPOM Medical Device Registration

3M ESPE monophase is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602512791. The device is manufactured by 3M DEUTSCHLAND GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 3M INDONESIA IMPORTAMA.

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Risk Class Kelas Resiko : B
3M ESPE monophase

3M ESPE Monophase

Analysis ID: AKL 20602512791

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. 3M INDONESIA IMPORTAMA

AR Address

KAWASAN PERKANTORAN HIJAU ARKADIA, TOWER F, LT.9, JL. TB. SIMATUPANG KAV. 88

Registration Date

Mar 22, 2022

Expiry Date

Sep 25, 2025

Product Type

Prosthetic Dental Equipment

Impression material.

Non Electromedic Non Sterile

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