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

PDS II (Polydioxanone) Monofilament Absorbable Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603604767. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
PDS II (Polydioxanone) Monofilament Absorbable Suture
Analysis ID: AKL 21603604767

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

Mar 15, 2023

Expiry Date

Feb 23, 2028

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

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