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STRYKER Hysteroscope Instrument - Indonesia BPOM Medical Device Registration

STRYKER Hysteroscope Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106910369. 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 Hysteroscope Instrument
Analysis ID: AKL 21106910369

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

Oct 28, 2024

Expiry Date

Dec 31, 2028

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Hysteroscope and accessories.

Non Electromedic Non Sterile

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