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ENDO-SCRUB® 2 SHEATH - Indonesia BPOM Medical Device Registration

ENDO-SCRUB® 2 SHEATH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703021675. The device is manufactured by MEDTRONIC XOMED INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
ENDO-SCRUB® 2 SHEATH
Analysis ID: AKL 20703021675

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

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

Jul 26, 2023

Expiry Date

Feb 07, 2028

Product Type

Ear, Nose and Throat Surgical Equipment

Nasopharyngoscope (flexible or rigid) and accessories.

Non Electromedic Sterile

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