TONTARRA THT Set - Indonesia BPOM Medical Device Registration

TONTARRA THT Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703917500. The device is manufactured by TONTARRA MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEDTEK.

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BPOM Registered

Risk Class Kelas Resiko : A

TONTARRA THT Set

Analysis ID: AKL 10703917500

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

TONTARRA MEDIZINTECHNIK GMBH

Country of Origin

Germany

Authorized Representative

MEDTEK

AR Address

Delta Building, Blok A-11, C-1 dan C-2, Jl. Suryopronoto No. 1-9

Registration Date

Oct 12, 2022

Expiry Date

Aug 30, 2027

Product Type

Ear, Nose and Throat Surgical Equipment

Ear, nose, and throat manual surgical instrument.

Non Electromedic Non Sterile

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TONTARRA THT Set - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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