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COVIDIEN Insufflator - Indonesia BPOM Medical Device Registration

COVIDIEN Insufflator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106712259. The device is manufactured by W.O.M. WORLD OF MEDICINE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTRONIC 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 : B
COVIDIEN Insufflator
Analysis ID: AKL 21106712259

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Feb 25, 2021

Expiry Date

Jan 13, 2026

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Laparoscopic insufflator.

Non Radiation Electromedics

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