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MANI Sutures Silk - Indonesia BPOM Medical Device Registration

MANI Sutures Silk is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603025642. The device is manufactured by MANI, INC. KIYOHARA FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FIXIPRIMA PERSADA.

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
MANI Sutures Silk
Analysis ID: AKL 21603025642

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. FIXIPRIMA PERSADA

AR Address

Jl. Pintu Air Raya No. 7, Blok B-5 Jakarta

Registration Date

Oct 12, 2021

Expiry Date

Aug 31, 2025

Product Type

Surgical Equipment

Natural nonabsorbable silk surgical suture.

Non Electromedic Sterile

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