EAGLE LABS LASIK Cannulae - Indonesia BPOM Medical Device Registration
EAGLE LABS LASIK Cannulae is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203023816. The device is manufactured by EAGLE LABS from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is UNIVERSAL STAR MULTILINK.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
EAGLE LABSCountry of Origin
United States
Authorized Representative
UNIVERSAL STAR MULTILINKAR Address
RUKO SERENADE CENTER BLOK A/27 JL.BOULEVARD GADING SERPONG TANGERANG 15810
Registration Date
Nov 18, 2021
Expiry Date
Jun 02, 2026
Product Type
Surgical Eye Equipment
Manual ophthalmic surgical instrument.
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