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MONOLAC Monofilament Glycolide-E-Caprolactone - Indonesia BPOM Medical Device Registration

MONOLAC Monofilament Glycolide-E-Caprolactone is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603717871. The device is manufactured by CHIRANA T. INJECTA S.R.O. from Czech Republic, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NUSA ASIA MEDIKA.

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 : C
MONOLAC Monofilament Glycolide-E-Caprolactone
Analysis ID: AKL 21603717871

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Czech Republic

Authorized Representative

PT. NUSA ASIA MEDIKA

AR Address

Rukan CBD, Green Lake City F No. 15 Ketapang. Cipondoh

Registration Date

Dec 01, 2021

Expiry Date

Aug 05, 2026

Product Type

Surgical Equipment

Absorbable poly(glycolide/ l -lactide) surgical suture.

Non Electromedic Sterile

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