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TERUMO ACD-A Solution - Indonesia BPOM Medical Device Registration

TERUMO ACD-A Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205311841. The device is manufactured by TERUMO PENPOL PRIVATE LTD from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO 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 : C
TERUMO ACD-A Solution
Analysis ID: AKL 20205311841

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. TERUMO INDONESIA

AR Address

Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta

Registration Date

Nov 22, 2022

Expiry Date

Jan 12, 2027

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Empty container for the collection and processing of blood and blood components.

Non Electromedic Sterile

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