TONTARRA IUD Kit - Indonesia BPOM Medical Device Registration

TONTARRA IUD Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103021776. 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 IUD Kit

Analysis ID: AKL 11103021776

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

Nov 17, 2022

Expiry Date

Aug 30, 2027

Product Type

Surgical Obstetric and Gynaecological Equipment

Obstetric-gynecologic general manual instrument.

Non Electromedic Non Sterile

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TONTARRA IUD Kit - 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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