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BEIEN Disposable Endoscopic Staplers and Reload Unit - Indonesia BPOM Medical Device Registration

BEIEN Disposable Endoscopic Staplers and Reload Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420727. The device is manufactured by WUXI BEIEN SURGERY DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GEM OF GRACE VIBRASA.

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BPOM Registered
Risk Class Kelas Resiko : C
BEIEN Disposable Endoscopic Staplers and Reload Unit
Analysis ID: AKL 21603420727

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GEM OF GRACE VIBRASA

AR Address

Ruko Perkantoran CBD Ciledug, Jl. HOS Cokroaminoto No. 93, Blok A3 No. 28-29, Kode Pos 15157, Kel. Karang Tengah, Kec. Karang Tengah, Kota Tangerang, Prov. Banten

Registration Date

Apr 01, 2024

Expiry Date

Jan 03, 2029

Product Type

Surgical Equipment

Implantable staple.

Non Electromedic Sterile

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