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RISE Polydioxanone Suture - Indonesia BPOM Medical Device Registration

RISE Polydioxanone Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222784. The device is manufactured by MEDIWIRE., CO. LTD from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.

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
RISE Polydioxanone Suture

STEIGEN Polydioxanone Suture

Analysis ID: AKL 21603222784

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEDIWIRE., CO. LTD

Country of Origin

Korea

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Sultan Iskandar Muda No. 7A & B

Registration Date

Nov 23, 2022

Expiry Date

Mar 03, 2027

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

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