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PENCYLCAP - Indonesia BPOM Medical Device Registration

PENCYLCAP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220207. The device is manufactured by B. BRAUN MEDICAL INDUSTRIES SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MERCK CHEMICALS AND LIFE SCIENCES.

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
PENCYLCAP
Analysis ID: AKL 20902220207

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. MERCK CHEMICALS AND LIFE SCIENCES

AR Address

Jl. TB Simatupang No 8 Pasar Rebo, Jakarta

Registration Date

Mar 09, 2022

Expiry Date

Sep 30, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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