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CARA SCREW Polydioxanone Suture - Indonesia BPOM Medical Device Registration

CARA SCREW Polydioxanone Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603716078. The device is manufactured by BUT CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HAJU MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
CARA SCREW Polydioxanone Suture
Analysis ID: AKL 21603716078

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

BUT CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. HAJU MEDICAL INDONESIA

AR Address

Gedung Tifa Arum Realty Lt.8, Suite 801 Jl. Kuningan Barat 1 No. 26, Kelurahan Kuningan Barat, Kecamatan Mampang Prapatan. Jakarta Selatan, DKI Jakarta

Registration Date

Feb 25, 2022

Expiry Date

Apr 15, 2024

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

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