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REMEDI Tourniquet - Indonesia BPOM Medical Device Registration

REMEDI Tourniquet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11604420028. The device is manufactured by HOSPITAL & HOMECARE IMP & EXP CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ANUGRAHMITRA SELARAS.

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
REMEDI Tourniquet
Analysis ID: AKL 11604420028

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. ANUGRAHMITRA SELARAS

AR Address

Jl. Agung Niaga IV Blok G.4 No. 54 Kel. Sunter Agung, Kec. Tanjung Priok, Jakarta Utara

Registration Date

Aug 05, 2024

Expiry Date

Jul 23, 2027

Product Type

Therapeutic Surgical Equipment

Nonpneumatic tourniquet.

Non Electromedic Non Sterile

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