Reference. 9430670-04ADU
Panda Patch™ Surgical Eye Protector for adults
Disposable polyethylene protector designed to safeguard the ocular area during surgery. It allows keeping the eyes closed and prevents ophthalmic injuries from occurring while the patient is anesthetized.
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Description
Panda Patch™ is an eye protector designed to safeguard the eyes during surgical intervention, thus preventing them from opening and causing corneal injuries or other ophthalmic complications while the patient is sedated. It is made of polyethylene, a flexible and resistant material that perfectly adapts to the eye socket and provides an effective protective barrier throughout the procedure. In addition, it comes with a tab for easy placement and removal, ensuring high practicality.
General Features
- An adhesive and disposable protector designed to safeguard the eyes during surgery
- Ergonomic shape, comfortably and practically adapts to the eye contour
- Biocompatible, hypoallergenic and latex-free composition for greater safety
- Easy and quick placement and removal thanks to its color-coded tab system
Composition
- Textured transparent film: polyethylene (PE)
- Adhesive: medical grade adhesive
- Red tab: polypropylene (PP)
Technical Specifications
- Length: 5.46 cm
- Width: 3.43 cm
- Tab color: red
- Compatibility: adult patients
Standards and Certifications
- MDR Regulation (EU) 2017/745, class I medical product
- EN ISO 13485:2016 (manufacturer)
General Features
- An adhesive and disposable protector designed to safeguard the eyes during surgery
- Ergonomic shape, comfortably and practically adapts to the eye contour
- Biocompatible, hypoallergenic and latex-free composition for greater safety
- Easy and quick placement and removal thanks to its color-coded tab system
Composition
- Textured transparent film: polyethylene (PE)
- Adhesive: medical grade adhesive
- Red tab: polypropylene (PP)
Technical Specifications
- Length: 5.46 cm
- Width: 3.43 cm
- Tab color: red
- Compatibility: adult patients
Standards and Certifications
- MDR Regulation (EU) 2017/745, class I medical product
- EN ISO 13485:2016 (manufacturer)








