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VERTEX BASIQ 20 - Indonesia BPOM Medical Device Registration

VERTEX BASIQ 20 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602320751. The device is manufactured by VERTEX DENTAL B.V from Netherlands, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PURE NOBLE SUN.

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Risk Class Kelas Resiko : B
VERTEX BASIQ 20
Analysis ID: AKL 20602320751

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VERTEX DENTAL B.V

Country of Origin

Netherlands

Authorized Representative

PURE NOBLE SUN

AR Address

Jl. Pecenongan No. 82 C, RT.002/RW.004, Kode Pos 10120, Kel. Kebon Kelapa, Kec. Gambir, Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta

Registration Date

Sep 20, 2023

Expiry Date

Aug 22, 2025

Product Type

Prosthetic Dental Equipment

Denture relining, repairing, or rebasing resin.

Non Electromedic Non Sterile

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