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SPINAUT - Indonesia BPOM Medical Device Registration

SPINAUT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403911066. The device is manufactured by IMEDICOM CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FAJAR SELARAS PARTNERS.

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
SPINAUT
Analysis ID: AKL 20403911066

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

IMEDICOM CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. FAJAR SELARAS PARTNERS

AR Address

Komplek Rukan PTC Blok 8C No. 28-29 Pulogadung Tel. 021-46827776 Fax. 021-46827033

Registration Date

Aug 28, 2023

Expiry Date

Dec 23, 2027

Product Type

Therapeutic Anesthesia Equipment

Anesthesia conduction catheter.

Non Electromedic Sterile

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