Auckland Medical Polymer(Tianjin) Co., Ltd.

Auckland Medical Polymer(Tianjin) Co., Ltd. holds 1 FDA 510(k) medical device clearance, cleared in 2020.

Top product codes for Auckland Medical Polymer(Tianjin) Co., Ltd.

GEI — General, Plastic Surgery1 device

Recent clearances by Auckland Medical Polymer(Tianjin) Co., Ltd.

K183148 — OKLand Patient Return Electrode PadCode GEI·2020-02-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.