Pure Global

AL Polydioxanone Sutures - Indonesia BPOM Medical Device Registration

AL Polydioxanone Sutures is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603814573. The device is manufactured by DONGWON MEDICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SOMETECH 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
AL Polydioxanone Sutures

AL Polydioxanone Suture

Analysis ID: AKL 21603814573

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. SOMETECH NEW Zealand

AR Address

AKR Tower Lantai 11 Unit 11G dan 11C, Jalan Panjang Nomor 5 ,RT 011 RW 010, Kec. Kebon Jeruk, Kel. Kebon Jeruk, Jakarta Barat, 11530

Registration Date

Sep 20, 2023

Expiry Date

Sep 07, 2027

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from DONGWON MEDICAL CO., LTD.
Products from the same manufacturer (1 products)