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RESYNO One Inj - Indonesia BPOM Medical Device Registration

RESYNO One Inj is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302320933. The device is manufactured by YOOYOUNG PHARMACEUTICAL CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ISCO LOGISTICS 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 : D
RESYNO One Inj
Analysis ID: AKL 31302320933

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Korea

Authorized Representative

PT. ISCO LOGISTICS INDONESIA

AR Address

JL. H.R. MOCH. MANGUNDIPROJO NO. 1A

Registration Date

Oct 04, 2023

Expiry Date

Jul 17, 2028

Product Type

Prosthetic Orthopedic Equipment

Intra articular fluid

Non Electromedic Sterile

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