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3M STERI-STRIP Skin Closures (Reinforced) - Indonesia BPOM Medical Device Registration

3M STERI-STRIP Skin Closures (Reinforced) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603422295. The device is manufactured by 3M COMPANY from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is BRIDGE TWO.

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
3M STERI-STRIP Skin Closures (Reinforced)
Analysis ID: AKL 11603422295

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

3M COMPANY

Country of Origin

United States

Authorized Representative

BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Oct 01, 2024

Expiry Date

Mar 22, 2029

Product Type

Surgical Equipment

Nonresorbable gauze/sponge for external use, sterile

Non Electromedic Sterile

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