🏭 Factory Campus: Shuangyang, Luojiang, Quanzhou, Fujian 🚢 Port of Shipment: Xiamen Port / Quanzhou Port, Fujian, China ISO 13485 / CE / FDA Registered
ISO 8 CLEANROOM Huifeng Maternity & Postpartum Care Pads Heavy Lochia Hospital specification sample showing multi-layer core construction and packaging options
⚡ 800 pcs/min Line
🛡️ IDIS6 Vision QC
🚢 FOB Xiamen
MODEL / SKU: HF-MP-HEAVY-LOCHIA-HOSPITAL

Huifeng Maternity & Postpartum Care Pads - Heavy Lochia Hospital

Commercial grade maternity & postpartum care pads specifically engineered for institutional healthcare procurement and private label consumer distribution. Manufactured in Quanzhou Huifeng's ISO 8 cleanroom facilities using high-speed full-servo automated lines running between 600 and 800 pieces per minute. Featuring certified virgin raw materials, Japanese Sumitomo superabsorbent polymer (SAP), and breathable microporous barrier films. Tested under ISO 11948-1 Rothwell retention standards to guarantee minimal surface rewet under sustained pressure. Fully certified under ISO 9001, ISO 13485, CE MDR Class I, and US FDA establishment listings with 3-day sample dispatch and custom master carton packaging shipped FOB Xiamen.

category Maternity & Postpartum Care Pads
moq 50,000 pcs
lead_time 15-20 days
port Xiamen Port, China
Size Heavy Lochia Hospital
Length 450 mm
Width 180 mm
Absorbency 700 ml
Features Extra-wide contour, looped ends or belt
Technical Manufacturing Dossier

OEM/ODM Contract Engineering & Quality Assurance Specs

Quanzhou Huifeng Sanitary Articles Co., Ltd. manufactures Huifeng Maternity & Postpartum Care Pads - Heavy Lochia Hospital to institutional healthcare and private-label contract specifications inside ISO Class 8 cleanrooms. Utilizing automated full-servo assembly lines operating up to 800 pieces per minute, each unit integrates Japanese Sumitomo superabsorbent polymer (SAP) and virgin Southern pine fluff pulp to achieve high retention capacity under ISO 11948-1 Rothwell mechanical pressure. In-line automated IDIS6 machine vision systems inspect 100% of finished units for foreign contaminants, structural symmetry, and elastic tensile integrity. Certified under CE MDR Class I, US FDA establishment registration, ISO 9001, and ISO 13485, all production runs undergo third-party CMA laboratory validation ensuring zero detectable fluorescent whitening agents and total microbial counts strictly under 20 CFU/g. Export orders are packaged in custom polybags or master cartons with 3-day initial sampling and rapid 15-day repeat production turnaround from Xiamen Port.

ISO 11948-1
Absorption Standard
< 20 CFU/g
Microbial Bioburden
3 Days
Sample Dispatch
15 Days
Repeat Production
Product Portfolio

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