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SURGIPRO Monofilament Polypropylene - Indonesia BPOM Medical Device Registration

SURGIPRO Monofilament Polypropylene is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603710533. The device is manufactured by COVIDIEN from Dominican, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
SURGIPRO Monofilament Polypropylene
Analysis ID: AKL 21603710533

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

COVIDIEN

Country of Origin

Dominican

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama

Registration Date

Dec 22, 2024

Expiry Date

Feb 20, 2029

Product Type

Surgical Equipment

Nonabsorbable polypropylene surgical suture.

Non Electromedic Sterile

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