Pure Global

SEILER Colposcope - Indonesia BPOM Medical Device Registration

SEILER Colposcope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106715744. The device is manufactured by SEILER INSTRUMENT & MANUFACTURING COMPANY, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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 : B
SEILER Colposcope
Analysis ID: AKL 21106715744

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Dec 22, 2021

Expiry Date

Oct 01, 2026

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Colposcope.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from SEILER INSTRUMENT & MANUFACTURING COMPANY, INC.
Products from the same manufacturer (3 products)