Pure Global

PDS* II (Polydioxanone) Suture - Indonesia BPOM Medical Device Registration

PDS* II (Polydioxanone) Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603012516. The device is manufactured by ETHICON, INC. from Mexico, 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
PDS* II (Polydioxanone) Suture
Analysis ID: AKL 21603012516

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ETHICON, INC.

Country of Origin

Mexico

Authorized Representative

PT. JOHNSON & JOHNSON NEW ZEALAND

AR Address

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

Registration Date

Jul 11, 2023

Expiry Date

Mar 14, 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