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SMITH & NEPHEW Opsite Flexifix - Indonesia BPOM Medical Device Registration

SMITH & NEPHEW Opsite Flexifix is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902715218. The device is manufactured by SMITH & NEPHEW MEDICAL LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ENSEVAL PUTERA MEGATRADING TBK.

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 : A
SMITH & NEPHEW Opsite Flexifix
Analysis ID: AKL 10902715218

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United Kingdom

Authorized Representative

PT. ENSEVAL PUTERA MEGATRADING TBK

AR Address

Jalan Pulo Lentut No.10 Kawasan Industri Pulogadung, Jakarta Timur

Registration Date

Sep 07, 2023

Expiry Date

Dec 31, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Medical adhesive tape and adhesive bandage

Non Electromedic Non Sterile

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