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MANI Surgical Eyed Needles - Indonesia BPOM Medical Device Registration

MANI Surgical Eyed Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603411338. The device is manufactured by MANI INC, KIYOHARA FACTORY. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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
MANI Surgical Eyed Needles
Analysis ID: AKL 11603411338

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

Jun 10, 2021

Expiry Date

Dec 31, 2024

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Non Sterile

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