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Trima Accel® LRS® Platelet, Plasma Set - Indonesia BPOM Medical Device Registration

Trima Accel® LRS® Platelet, Plasma Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320508. The device is manufactured by TFB MANUFACTURING SRL from Costa Rica, 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
Trima Accel® LRS® Platelet, Plasma Set
Analysis ID: AKL 20209320508

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Costa Rica

Authorized Representative

PT. TERUMO INDONESIA

AR Address

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

Registration Date

Oct 01, 2024

Expiry Date

May 17, 2029

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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