URGOTUL ABSORB - Indonesia BPOM Medical Device Registration
URGOTUL ABSORB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603221348. The device is manufactured by URGO LABORATORIES from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is WICAKSANA OVERSEAS INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
URGO LABORATORIESCountry of Origin
France
Authorized Representative
WICAKSANA OVERSEAS INTERNATIONALAR Address
Jl. Ancol Barat VII Blok A 5D No. 2 RT.006/RW.001, Kel. Ancol, Kec. Pademangan, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta
Registration Date
Aug 05, 2024
Expiry Date
Dec 31, 2026
Product Type
Surgical Equipment
Occlusive Wound Dressing
Non Electromedic Non Sterile
HUMER Blocked Nose โ 100% sea water โ nasal spray
URGOTUL
URGOTUL Absorb Border
HUMER Nasal Hygiene-100% sea water-Nasal Spray (Children)
URGOTUL Ag/Silver
HUMER STOP VIRUS โ Nasal Spray
Suprasorb H
VANTELIN SUPPORT THUMB ARMOR
IIDA HOSIERY CO., LTD.
TRANSFORM Occlusion Ballon Catheter
STRYKER NEUROVASCULAR
SYNCHRO2 Guidewire
STRYKER NEUROVASCULAR
EASY LINE One Step Ovulation Test (Strip)
HUBEI MEIBAO BIOTECHNOLOGY CO., LTD.
ONETOUCH ULTRA PLUS TEST STRIP
LIFESCAN SCOTLAND LIMITED

