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SANLI Vacuum Blood Collection Tubes for Single Use, Lithium Heparin Tube - Indonesia BPOM Medical Device Registration

SANLI Vacuum Blood Collection Tubes for Single Use, Lithium Heparin Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101125010. The device is manufactured by LIUYANG SANLI MEDICAL TECHNOLOGY DEVELOPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PYRIDAM FARMA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
SANLI Vacuum Blood Collection Tubes for Single Use, Lithium Heparin Tube
Analysis ID: AKL 20101125010

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PYRIDAM FARMA

AR Address

Sinarmas MSIG Tower Lt. 12 Jl. Jenderal Sudirman Kav. 21 Kelurahan Karet

Registration Date

Aug 13, 2021

Expiry Date

Apr 01, 2025

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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