Pure Global

DAKO PD-L1 IHC 22C3 pharmDx - Indonesia BPOM Medical Device Registration

DAKO PD-L1 IHC 22C3 pharmDx is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201420075. The device is manufactured by AGILENT TECHNOLOGIES, INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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
DAKO PD-L1 IHC 22C3 pharmDx
Analysis ID: AKL 10201420075

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 5 Jl. Tentara Pelajar No. 5

Registration Date

May 08, 2024

Expiry Date

Oct 19, 2025

Product Type

Biological Dyes

Immunohistochemistry reagents and kits (Qualitative).

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from AGILENT TECHNOLOGIES, INC
Products from the same manufacturer (1 products)