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 21106715889. 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
SEILER INSTRUMENT & MANUFACTURING COMPANY, INC.Country of Origin
United States
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Dec 24, 2021
Expiry Date
Oct 01, 2026
Product Type
Diagnostic Obstetric and Gynaecological Equipment
Colposcope.
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