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FUJITA Forceps Instrument - Indonesia BPOM Medical Device Registration

FUJITA Forceps Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603421918. The device is manufactured by TAKASAGO MEDICAL INDUSTRY CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is AKSATA MARGA MAKMUR.

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
FUJITA Forceps Instrument
Analysis ID: AKL 11603421918

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

AKSATA MARGA MAKMUR

AR Address

Foresta Business Loft 6 Unit 1, BSD City

Registration Date

Aug 21, 2024

Expiry Date

Jun 12, 2029

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Non Sterile

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