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ECLERIS Colposcope - Indonesia BPOM Medical Device Registration

ECLERIS Colposcope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106125916. The device is manufactured by ECLERIS USA from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SOMETECH NEW Zealand.

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 : B
ECLERIS Colposcope
Analysis ID: AKL 21106125916

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ECLERIS USA

Country of Origin

United States

Authorized Representative

PT. SOMETECH NEW Zealand

AR Address

AKR Tower Lantai 11 Unit 11G, Jl. Panjang No. 5

Registration Date

Sep 22, 2021

Expiry Date

Mar 22, 2026

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Colposcope.

Non Radiation Electromedics

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