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3M ESPE VITREBOND Light Cure Glass Ionomer Liner / - Indonesia BPOM Medical Device Registration

3M ESPE VITREBOND Light Cure Glass Ionomer Liner / is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602513787. The device is manufactured by 3M ESPE DENTAL PRODUCTS from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 3M INDONESIA IMPORTAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
3M ESPE VITREBOND Light Cure Glass Ionomer Liner /
Analysis ID: AKL 20602513787

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. 3M INDONESIA IMPORTAMA

AR Address

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

Registration Date

Feb 25, 2020

Expiry Date

Jan 31, 2024

Product Type

Prosthetic Dental Equipment

Dental cement.

Non Electromedic Non Sterile

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