Pure Global

Endcare Dilator Sheath - Indonesia BPOM Medical Device Registration

Endcare Dilator Sheath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420109. The device is manufactured by BM KOREA CO. LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
Endcare Dilator Sheath

ENDOCARE DILATOR SHEATH

Analysis ID: AKL 11303420109

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

BM KOREA 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

Mar 13, 2024

Expiry Date

Jun 30, 2027

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from BM KOREA CO. LTD.
Products from the same manufacturer (1 products)