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ENDOLOOP Ligature made with PDS II (Polydioxanone) Suture - Indonesia BPOM Medical Device Registration

ENDOLOOP Ligature made with PDS II (Polydioxanone) Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420710. The device is manufactured by JOHNSON & JOHNSON DO BRASIL IND. COM. DE PROD. P/ SAUDE LTDA from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is JOHNSON AND JOHNSON INDONESIA TWO.

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BPOM Registered
Risk Class Kelas Resiko : C
ENDOLOOP Ligature made with PDS II (Polydioxanone) Suture
Analysis ID: AKL 21603420710

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

JOHNSON AND JOHNSON INDONESIA TWO

AR Address

K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A.

Registration Date

Mar 28, 2024

Expiry Date

Jan 23, 2029

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

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