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K2 Blood Tube Stripper - Indonesia BPOM Medical Device Registration

K2 Blood Tube Stripper is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203420201. The device is manufactured by W-ESPR TECHNOLOGY CO LTD from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FRISMED HOSLAB 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 : A
K2 Blood Tube Stripper
Analysis ID: AKL 10203420201

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Taiwan (China)

Authorized Representative

PT. FRISMED HOSLAB INDONESIA

AR Address

Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321

Registration Date

Dec 19, 2024

Expiry Date

Aug 12, 2028

Product Type

Pathology Equipment and Accessories

Device for sealing microsections. (Non Electrically Operated)

Non Electromedic Non Sterile

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