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Definisse™ Restore Filler + Lidocaine - Indonesia BPOM Medical Device Registration

Definisse™ Restore Filler + Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602122506. The device is manufactured by CROMA-PHARMA GMBH from Austria, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TRANSFARMA MEDICA INDAH.

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BPOM Registered
Risk Class Kelas Resiko : D
Definisse™ Restore Filler + Lidocaine
Analysis ID: AKL 31602122506

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

CROMA-PHARMA GMBH

Country of Origin

Austria

Authorized Representative

PT. TRANSFARMA MEDICA INDAH

AR Address

Unit 802, 8th Fl., Wisma Pondok Indah 2 JL. Sultan Iskandar Muda Kav V - TA, Pondok Indah.

Registration Date

May 05, 2021

Expiry Date

Jul 30, 2025

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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