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ROUSEMED Forceps (Part 1) - Indonesia BPOM Medical Device Registration

ROUSEMED Forceps (Part 1) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603323910. The device is manufactured by ROUSEMED from Pakistan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INNOVATION HEALTHCARE 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 : A
ROUSEMED Forceps (Part 1)
Analysis ID: AKL 11603323910

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

ROUSEMED

Country of Origin

Pakistan

Authorized Representative

PT. INNOVATION HEALTHCARE INDONESIA

AR Address

Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450

Registration Date

May 04, 2023

Expiry Date

Jan 01, 2028

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Non Sterile

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