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VICRYL Rapide® Polyglactin 910 - Indonesia BPOM Medical Device Registration

VICRYL Rapide® Polyglactin 910 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603704887. The device is manufactured by JOHNSON & JOHNSON MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. JOHNSON & JOHNSON 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 : C
VICRYL Rapide® Polyglactin 910
Analysis ID: AKL 21603704887

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. JOHNSON & JOHNSON NEW ZEALAND

AR Address

K-Link Tower Lt. 12, Jln. Jend. Gatot Subroto Kav. 59 A

Registration Date

Jun 20, 2023

Expiry Date

Jan 23, 2027

Product Type

Surgical Equipment

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

Non Electromedic Sterile

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