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NEAUVIA INTENSE RHEOLOGY - Indonesia BPOM Medical Device Registration

NEAUVIA INTENSE RHEOLOGY is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420057. The device is manufactured by MATEX LAB SPA from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
NEAUVIA INTENSE RHEOLOGY
Analysis ID: AKL 31602420057

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MATEX LAB SPA

Country of Origin

Italy

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan

Registration Date

May 30, 2024

Expiry Date

Feb 15, 2028

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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