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ANGELUS INTERLIG - Indonesia BPOM Medical Device Registration

ANGELUS INTERLIG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420465. 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. LIGHTNING JAYA 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 : C
ANGELUS INTERLIG
Analysis ID: AKL 20602420465

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

PT. LIGHTNING JAYA INDONESIA

AR Address

Jalan Moh. Toha Nomor H-28, Kilometer 06, RT. 002/RW. 007, Kel. Periuk, Kec. Periuk, Kota Tangerang, Prov. Banten

Registration Date

Dec 16, 2024

Expiry Date

Jun 05, 2029

Product Type

Prosthetic Dental Equipment

Endodontic stabilizing splint.

Non Electromedic Non Sterile

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