EPPENDORF Reference 2 Adjustable - Indonesia BPOM Medical Device Registration
EPPENDORF Reference 2 Adjustable is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102411529. The device is manufactured by EPPENDORF SE. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
EPPENDORF SE.Country of Origin
Germany
Authorized Representative
PT. ENSEVAL MEDIKA PRIMAAR Address
JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG
Registration Date
Sep 20, 2023
Expiry Date
Dec 31, 2026
Product Type
Clinical Laboratory Equipment
Pipetting and diluting system for clinical use.
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