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SAYPHA FILLER Lidocaine - Indonesia BPOM Medical Device Registration

SAYPHA FILLER Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602918914. 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. QUALTEK CONSULTANT JAKARTA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : D
SAYPHA FILLER Lidocaine
Analysis ID: AKL 31602918914

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

CROMA-PHARMA GMBH

Country of Origin

Austria

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Nov 04, 2020

Expiry Date

Aug 30, 2024

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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