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WEGO OXYGENATOR - Indonesia BPOM Medical Device Registration

WEGO OXYGENATOR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504420072. The device is manufactured by SHANDONG WEGO TUOWEI MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRANSMEDIC 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 : C
WEGO OXYGENATOR
Analysis ID: AKL 20504420072

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TRANSMEDIC INDONESIA

AR Address

Perkantoran Menara Era Unit G-01 JL.Senen Raya No.135-137 RT 00 RW 00, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Senen, Kel. Senen

Registration Date

Aug 30, 2024

Expiry Date

Feb 28, 2029

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass oxygenator.

Non Electromedic Sterile

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