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CELTRA Universal - Indonesia BPOM Medical Device Registration

CELTRA Universal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602412655. The device is manufactured by DENTSPLY CERAMCO. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DENTSPLY SIRONA INDONESIA.

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 : B
CELTRA Universal
Analysis ID: AKL 20602412655

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DENTSPLY CERAMCO.

Country of Origin

United States

Authorized Representative

PT. DENTSPLY SIRONA INDONESIA

AR Address

Tempo Scan Tower 28th Floor, Jl. HR. Rasuna Said Kav.3-4 Kel. Kuningan Timur Kec. Setia Budi, Jakarta Selatan 12950

Registration Date

Nov 29, 2019

Expiry Date

May 07, 2024

Product Type

Prosthetic Dental Equipment

Dental cement.

Non Electromedic Non Sterile

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