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VDW. ULTRA® - Indonesia BPOM Medical Device Registration

VDW. ULTRA® is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603712620. The device is manufactured by SATELEC A COMPANY OF ACTEON GROUP. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. THOMASONG NIRMALA.

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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Risk Class Kelas Resiko : B
VDW. ULTRA®

VDW.ULTRA®

Analysis ID: AKL 20603712620

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

France

Authorized Representative

PT. THOMASONG NIRMALA

AR Address

JL. AM SANGAJI NO. 20A KEL. PETOJO UTARA, KEC. GAMBIR JAKARTA TELP. 021-63855888

Registration Date

Jul 09, 2021

Expiry Date

Jan 07, 2024

Product Type

Surgical Dental Equipment

Ultrasonic scaler.

Non Radiation Electromedics

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