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SENDOLINE Paste Filler - Indonesia BPOM Medical Device Registration

SENDOLINE Paste Filler is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603716658. The device is manufactured by SENDOLINE. from Sweden, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. COBRA DENTAL 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 : A
SENDOLINE Paste Filler
Analysis ID: AKL 10603716658

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

SENDOLINE.

Country of Origin

Sweden

Authorized Representative

PT. COBRA DENTAL INDONESIA

AR Address

Jl. Pakuningratan No. 69

Registration Date

Dec 09, 2019

Expiry Date

Sep 16, 2024

Product Type

Surgical Dental Equipment

Dental hand instrument.

Non Electromedic Non Sterile

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