Fluorescein Sodium Ophthalmic Test Strips

Fluorescein Sodium Ophthalmic Test Strips — single-use strips made of filter paper impregnated with orange-red fluorescein sodium, with a ha

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Medical Device

Fluorescein Sodium Ophthalmic Test Strips

Fluorescein Sodium Ophthalmic Test Strips — single-use strips made of filter paper impregnated with orange-red fluorescein sodium, with a hand-held grip. Clinically used for examination of corneal and ocular-surface epithelial cell damage (corneal staining under cobalt blue light). Executive standard: Q/MZL001-2024. Brand: Qianwanli. GMP manufactured by Artemisine Medicines Technology with full batch documentation.

Product NameFluorescein Sodium Ophthalmic Test Strips
Dosage FormDiagnostic Strip (Medical Device)
Strength1 strip per pouch — filter paper impregnated with orange-red fluorescein sodium, with handle
StandardsBP / ENTERPRISE
Packing1 strip/pouch; 10 pouches/box; 20 boxes/middle box; 50 middle boxes/carton
DocumentsCOA, COPP, DMF, CTD Dossiers
MOQContact us for MOQ and current stock
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WHO Prescribing Guidance

Indications · Administration · Dosage · Precautions

Reference information summarised from WHO prescribing guidance. Expand each item below — clinical use must always follow the locally approved product insert.

🎯Indications▾
Topical ophthalmic treatment as stated on the product label — infection, inflammation or ocular surface support (see the registered indication for your market).
💧Administration▾
Instil into the conjunctival sac using aseptic technique; discard the container 4 weeks after first opening and never share eye drops between patients.
⚖️Dosage▾
Usually 1–2 drops 3–4 times daily, or as directed by the prescriber; follow the product insert for the specific active substance.
⚠️Precautions & Warnings▾
For topical ocular use only. Stop and seek advice if pain, worsening vision or persistent redness develops; avoid contact lenses during treatment.

Reference: WHO Model Formulary / WHO Model List of Essential Medicines. For professional reference only — clinical use must follow the locally approved product insert and national treatment guidelines.

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