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TRICELL PRP Kit - Indonesia BPOM Medical Device Registration

TRICELL PRP Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206914854. The device is manufactured by REV-MED INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HARMONI PRIMA MEDIKA.

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 : B
TRICELL PRP Kit
Analysis ID: AKL 20206914854

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

REV-MED INC.

Country of Origin

Korea

Authorized Representative

PT. HARMONI PRIMA MEDIKA

AR Address

Jl. Tanjung Selor No. 1A, Cideng, Gambir, Jakarta Pusat, 10150

Registration Date

Feb 07, 2024

Expiry Date

Dec 12, 2028

Product Type

Manual Hematology Equipment

Platelet aggregometer.

Invitro Diagnostics

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