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VACUETTE ESR Pipette - Indonesia BPOM Medical Device Registration

VACUETTE ESR Pipette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206913615. The device is manufactured by JP SELECTA, AT AQUISEL from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SABA INDOMEDIKA.

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
VACUETTE ESR Pipette
Analysis ID: AKL 20206913615

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Spain

Authorized Representative

SABA INDOMEDIKA

AR Address

Ruko Kedoya Elok Plaza DB-33 Jl. Panjang No.7-9

Registration Date

May 08, 2024

Expiry Date

Jul 02, 2026

Product Type

Manual Hematology Equipment

Erythrocyte sedimentation rate test (other, manually operated)

Invitro Diagnostics

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