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TECHCORD SAFEFUSER - Indonesia BPOM Medical Device Registration

TECHCORD SAFEFUSER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220550. The device is manufactured by TECHCORD CO.,LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SKBIO NUSA MEDICA.

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
TECHCORD SAFEFUSER
Analysis ID: AKL 20902220550

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TECHCORD CO.,LTD.

Country of Origin

Korea

Authorized Representative

PT. SKBIO NUSA MEDICA

AR Address

KOMPLEK WIJAYA GRAHA PURI BLOK G NO. 17 LT. 3 JL. WIJAYA II, KEL. PULO KEC. KEBAYORAN BARU JAKARTA SELATAN

Registration Date

Jun 10, 2022

Expiry Date

Jan 13, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Electromedic Non Sterile

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