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TEKNA Modular Rectangular 6000 Series Multiplace Hyperbaric Chamber - Indonesia BPOM Medical Device Registration

TEKNA Modular Rectangular 6000 Series Multiplace Hyperbaric Chamber is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321404. The device is manufactured by TEKNA MANUFACTURING PVT. LTD from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DS SOLUTIONS INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : C
TEKNA Modular Rectangular 6000 Series Multiplace Hyperbaric Chamber
Analysis ID: AKL 20403321404

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

DS SOLUTIONS INTERNATIONAL

AR Address

Jl. Arteri Kelapa Gading, Rukan The FIFTY No. 6-7 RT. 001 RW. 001 Kelurahan Pegangsaan Dua

Registration Date

Jul 11, 2023

Expiry Date

Mar 22, 2026

Product Type

Therapeutic Anesthesia Equipment

Hyperbaric chamber.

Non Radiation Electromedics

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