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LIGAFIX 30 Resorbable Interference Screw - Indonesia BPOM Medical Device Registration

LIGAFIX 30 Resorbable Interference Screw is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21303612213. The device is manufactured by S.B.M. S.A.S. from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ENDO 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
LIGAFIX 30 Resorbable Interference Screw
Analysis ID: AKL 21303612213

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

S.B.M. S.A.S.

Country of Origin

France

Authorized Representative

PT. ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

May 13, 2024

Expiry Date

Jun 20, 2027

Product Type

Prosthetic Orthopedic Equipment

Single/multiple component metallic bone fixation appliances and accessories.

Non Electromedic Sterile

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