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CapnoPen CP-001k - Indonesia BPOM Medical Device Registration

CapnoPen CP-001k is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420284. The device is manufactured by CAPNOPHARM GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PACIFIC SAINTIFINDO.

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
CapnoPen CP-001k
Analysis ID: AKL 20801420284

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CAPNOPHARM GMBH

Country of Origin

Germany

Authorized Representative

PT. PACIFIC SAINTIFINDO

AR Address

Komplek Green Lake City Rukan Crown Blok C nomor 27 RT 012 RW 011 Kel. Petir Kec. Cipondoh, Tangerang, Provinsi Banten 15147

Registration Date

Aug 01, 2024

Expiry Date

Jan 15, 2029

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Electromedic Sterile

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