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XISHAN Single-use Sterile Cranial Perforator - Indonesia BPOM Medical Device Registration

XISHAN Single-use Sterile Cranial Perforator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002024309. The device is manufactured by CHONGQING XISHAN SCIENCE & TECHNOLOGY CO., LTD from China, 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
XISHAN Single-use Sterile Cranial Perforator
Analysis ID: AKL 21002024309

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

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

Feb 10, 2023

Expiry Date

Oct 20, 2027

Product Type

Surgical Neurology Equipment

Powered simple cranial drills, burrs, trephines, and their accessories.

Non Electromedic Sterile

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