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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
W.O.M. WORLD OF MEDICINE GMBH.Country of Origin
Germany
Authorized Representative
MEDTRONIC INDONESIAAR 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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