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INTERLIG Impragnated Glass Fiber - Indonesia BPOM Medical Device Registration

INTERLIG Impragnated Glass Fiber is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602511466. The device is manufactured by ANGELUS INDUSTRIA DE PRODUTOS ODONTOLOGICOS S/A from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BINTANG SAUDARA SEMESTA JAYA.

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 : C
INTERLIG Impragnated Glass Fiber
Analysis ID: AKL 20602511466

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

PT. BINTANG SAUDARA SEMESTA JAYA

AR Address

Jl.Asia No.212 A-B, Medan

Registration Date

Aug 17, 2023

Expiry Date

Jul 10, 2028

Product Type

Prosthetic Dental Equipment

Endodontic stabilizing splint.

Non Electromedic Non Sterile

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