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SEEKARY Sedimentation Buffer Solution - Indonesia BPOM Medical Device Registration

SEEKARY Sedimentation Buffer Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204420290. The device is manufactured by HANGZHOU TESTSEA BIOTECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FLEXYLABS INSTRUMENT INDONESIA.

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 : A
SEEKARY Sedimentation Buffer Solution
Analysis ID: AKL 10204420290

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. FLEXYLABS INSTRUMENT INDONESIA

AR Address

Ruko Symphony Harapan Indah Blok HX1 No.12 Kota Harapan Indah, Kel. Pusaka Rakyat, Kec. Tarumajaya, Kab. Bekasi, Jawa Barat

Registration Date

Nov 22, 2024

Expiry Date

Jun 04, 2029

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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