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STRYKER Arthroscopes Instrument - Indonesia BPOM Medical Device Registration

STRYKER Arthroscopes Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801715918. The device is manufactured by STRYKER ENDOSCOPY. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
STRYKER Arthroscopes Instrument
Analysis ID: AKL 20801715918

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

STRYKER ENDOSCOPY.

Country of Origin

United States

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

Jun 28, 2024

Expiry Date

Feb 06, 2028

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Electromedic Sterile

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