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SENDOLINE Finger Plugs - Indonesia BPOM Medical Device Registration

SENDOLINE Finger Plugs is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603716493. The device is manufactured by SENDOLINE. from Sweden, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is COBRA DENTAL INDONESIA.

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Risk Class Kelas Resiko : A
SENDOLINE Finger Plugs

SENDOLINE Finger Plugger

Analysis ID: AKL 10603716493

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

SENDOLINE.

Country of Origin

Sweden

Authorized Representative

COBRA DENTAL INDONESIA

AR Address

Jl. Pakuningratan No. 69

Registration Date

Feb 14, 2022

Expiry Date

Sep 16, 2024

Product Type

Surgical Dental Equipment

Dental hand instrument.

Non Electromedic Non Sterile

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