Pure Global

Onemed Silicone Impression Material - Indonesia BPOM Medical Device Registration

Onemed Silicone Impression Material is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420395. The device is manufactured by SHANGHAI BEYZEN BIOLOGICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTIGLOBAL PERFECT RESULT SOURCE.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
Onemed Silicone Impression Material
Analysis ID: AKL 20602420395

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INTIGLOBAL PERFECT RESULT SOURCE

AR Address

KOMPLEK DARMO PARK II BLOK 4/14

Registration Date

Oct 07, 2024

Expiry Date

Oct 04, 2027

Product Type

Prosthetic Dental Equipment

Impression material.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from SHANGHAI BEYZEN BIOLOGICAL TECHNOLOGY CO., LTD
Products from the same manufacturer (3 products)