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SLEE Vacuum Tissue Processor (MTM) and Accessories - Indonesia BPOM Medical Device Registration

SLEE Vacuum Tissue Processor (MTM) and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203220039. The device is manufactured by SLEE MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MAIN VANADIA.

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BPOM Registered
Risk Class Kelas Resiko : A
SLEE Vacuum Tissue Processor (MTM) and Accessories
Analysis ID: AKL 10203220039

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

SLEE MEDICAL GMBH

Country of Origin

Germany

Authorized Representative

PT. MAIN VANADIA

AR Address

SENTRA INDUSTRI TERPADU PANTAI INDAH KAPUK BLOK G1 NO. 5 JAKARTA UTARA 14470

Registration Date

Dec 31, 2024

Expiry Date

Aug 02, 2029

Product Type

Pathology Equipment and Accessories

Tissue processing equipment (electrically operated)

Invitro Diagnostics

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