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TERUMO Syringe 60 ml - Indonesia BPOM Medical Device Registration

TERUMO Syringe 60 ml is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902916582. The device is manufactured by TERUMO (PHILIPPINES) CORPORATION from Philippines, and is classified as Risk Class Kelas Resiko : B. 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 : B
TERUMO Syringe 60 ml
Analysis ID: AKL 20902916582

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Philippines

Authorized Representative

PT. TERUMO INDONESIA

AR Address

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

Registration Date

Aug 13, 2024

Expiry Date

Jul 08, 2029

Product Type

Therapeutic General and Individual Hospital Equipment

Piston syringe.

Non Electromedic Sterile

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