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ENLITE Serter- MMT 7510 - Indonesia BPOM Medical Device Registration

ENLITE Serter- MMT 7510 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902612168. The device is manufactured by MEDTRONIC MINIMED from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
ENLITE Serter- MMT 7510
Analysis ID: AKL 20902612168

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEDTRONIC MINIMED

Country of Origin

United States

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

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

Registration Date

May 06, 2020

Expiry Date

Mar 12, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Non Sterile

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