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TECHCORD ENDOSCOPIC DILATOR SHEATH - Indonesia BPOM Medical Device Registration

TECHCORD ENDOSCOPIC DILATOR SHEATH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303320381. The device is manufactured by TECHCORD CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is 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 : A
TECHCORD ENDOSCOPIC DILATOR SHEATH
Analysis ID: AKL 11303320381

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

TECHCORD CO., LTD.

Country of Origin

Korea

Authorized Representative

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

May 08, 2023

Expiry Date

Jan 30, 2028

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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