RIESTER – Metpak - Indonesia BPOM Medical Device Registration
RIESTER – Metpak is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902025260. The device is manufactured by RUDOLF RIESTER GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is LABORA MANDIRI INDO PRATAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
RUDOLF RIESTER GMBHCountry of Origin
Germany
Authorized Representative
LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47
Registration Date
Sep 11, 2020
Expiry Date
Jun 16, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Pressure infusor for an I.V. bag.
Non Electromedic Non Sterile
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