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VOLUME INSTRUMENTS - Indonesia BPOM Medical Device Registration

VOLUME INSTRUMENTS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420054. The device is manufactured by MEDYTOX INC from Korea, 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
VOLUME INSTRUMENTS

ATIERE Volume

Analysis ID: AKL 31602420054

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MEDYTOX INC

Country of Origin

Korea

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

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

Registration Date

Jun 12, 2024

Expiry Date

Jan 23, 2029

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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