75% Silver Nitrate Applicator Sticks with Wooden Shafts
AGNAVELIS Silver Nitrate Applicator Sticks are non-sterile, single-use applicators with a tip containing 75% silver nitrate and 25% potassium nitrate on a rigid wooden shaft. They are intended for controlled, localised chemical cauterisation of small, clearly defined superficial tissue areas by trained healthcare professionals.
The sticks are supplied in applicator stick format as individually packed sticks, presented in the AGNAVELIS packaging tube. The rigid wooden shaft is designed to support controlled and precise placement of the treated tip. The product is a Class I medical device manufactured by Genco Tıbbi Cihazlar San. Tic. Ltd. Şti. in Türkiye, and it is intended for professional use only.
Product Specification
Every value below is taken from the product label, the product brochure or the current Instructions for Use.
| Product name | AGNAVELIS Silver Nitrate Applicator Sticks |
|---|---|
| Brand | AGNAVELIS |
| Active tip composition | 75% silver nitrate / 25% potassium nitrate |
| Applicator shaft | Rigid wooden shaft |
| Device status | Medical device, Class I |
| Sterility | Non-sterile |
| Reuse | Single use — do not reuse, reprocess or re-sterilise |
| Presentation | Applicator stick format, individually packed sticks |
| Intended users | Trained healthcare professionals |
| Intended purpose | Controlled, localised chemical cauterisation of small, clearly defined superficial tissue areas |
| Legal manufacturer | Genco Tıbbi Cihazlar San. Tic. Ltd. Şti. |
| Country of manufacture | Türkiye |
| Storage | Store dry, protected from light, in the original packaging |
| Reference documentation | Instructions for Use IFU-AGN-00, Rev. 00 (English and Turkish) |
Applicator length, pack quantity, catalogue references and expiry data are confirmed per order and per market. Send an enquiry to receive the current packaging and reference details for your destination country.
Intended Purpose
The product is intended to provide controlled, localised chemical cauterisation of small and clearly defined superficial tissue areas. Clinical use must remain within the indications supported by the manufacturer's technical documentation.
- Chemical cauterisation of small superficial bleeding sites.
- Controlled reduction of excessive granulation or hypergranulation tissue.
- Clinically appropriate localised applications in wound and stoma care.
- Other small superficial lesions where localised cauterisation is considered appropriate by a healthcare professional.
Intended Users and Patients
Intended user: trained healthcare professionals.
Patient population: patients for whom localised chemical cauterisation is clinically indicated. Use in paediatric patients, or during pregnancy or breastfeeding, should follow an individual professional clinical assessment.
Contraindications
- Known hypersensitivity to silver nitrate or potassium nitrate.
- Uncertain, atypically coloured or shaped lesions, or lesions suspected of malignancy, unless assessed by an appropriate physician.
- Direct application to the eye or peri-ocular tissues.
- Use over large body surface areas, on deep tissues, or outside the intended purpose.
Warnings Summary
Summarised from the current Instructions for Use. The complete warnings and precautions, application instructions and first-aid information are given in the IFU, which takes precedence over any summary on this page.
- For professional use only.
- The product is non-sterile. Do not use where the procedure requires a sterile device.
- Single use only. Do not reuse, reprocess or re-sterilise.
- Do not touch the active tip with bare or wet hands. Wear appropriate gloves, and eye protection where indicated.
- Limit contact with healthy tissue; silver nitrate may cause chemical irritation and dark staining of healthy skin.
- Protect clothing, work surfaces and equipment, because silver nitrate may cause persistent brown-black stains.
- When used in or near the mouth, prevent ingestion of fragments of the active tip.
- Keep out of reach of children.
- Do not use if the packaging is damaged or wet, or if the product shows visible deterioration.
Storage Information
- Store dry, protected from light and in the original packaging.
- After opening, reseal the remaining product securely and protect it from moisture.
- The expiry date is stated on the label. Do not use after the expiry date.
Complete Instructions for Use
IFU-AGN-00, Rev. 00, issued 03.09.2026. English and Turkish in one document.
Wooden and Flexible Plastic Applicator Formats
AGNAVELIS uses a rigid wooden shaft. Some products in the international market use flexible plastic applicators. Buyers should select the format appropriate to their professional requirements.
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