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COVIDIEN Pump - Indonesia BPOM Medical Device Registration

COVIDIEN Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106712260. 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 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 Pump
Analysis ID: AKL 21106712260

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

MEDTRONIC INDONESIA

AR Address

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

Registration Date

Feb 22, 2021

Expiry Date

Jan 13, 2026

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Gynecologic laparoscope and accessories.

Non Radiation Electromedics

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