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GEOTEK Maxicore-U Automatic Reusable Biopsy Gun - Indonesia BPOM Medical Device Registration

GEOTEK Maxicore-U Automatic Reusable Biopsy Gun is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801122671. The device is manufactured by GEOTEK MEDIKAL VE SAGLIK HIZMETLERI TIC. SAN. LTD. ลžTI from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ABADINUSA USAHASEMESTA.

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BPOM Registered
Risk Class Kelas Resiko : C
GEOTEK Maxicore-U Automatic Reusable Biopsy Gun
Analysis ID: AKL 20801122671

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

ABADINUSA USAHASEMESTA

AR Address

Jalan Raden Saleh No. 45 G

Registration Date

May 06, 2021

Expiry Date

Mar 05, 2024

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument (electric)

Non Electromedic Non Sterile

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