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BOP TI Sterilization Pouches and Reels - Indonesia BPOM Medical Device Registration

BOP TI Sterilization Pouches and Reels is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903420160. The device is manufactured by SPS MEDICAL from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is LABORA MANDIRI INDO PRATAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
BOP TI Sterilization Pouches and Reels
Analysis ID: AKL 20903420160

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SPS MEDICAL

Country of Origin

France

Authorized Representative

LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47, RT.014, RW.003, Desa/Kelurahan Terban, Kecamanan Gondokusuman, Kota Yogyakarta, Provinsi Daerah Istimewa Yogyakarta, Kode Pos : 55223

Registration Date

Feb 17, 2024

Expiry Date

Nov 16, 2026

Product Type

General Hospital Equipment and Other Individuals

Sterilization wrap.

Non Electromedic Non Sterile

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