- Condition: Factory New
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Learn more:
- MFR: Integra Lifesciences Ships from MFI Medical
- MPN: 30-RS3
Frequently asked questions
Is this pessary suitable for clinical support?
Yes, the Integra Miltex Ring Pessary is specifically engineered for clinical pelvic support applications. It is a professional-grade medical device designed to assist in the management of pelvic organ prolapse.
Is this a high-quality medical device?
Absolutely. It is manufactured by Integra Lifesciences, a highly trusted name in surgical instruments. This ensures that every unit is crafted with the precision and consistency required for professional healthcare settings.
Does this meet institutional regulatory standards?
Yes, this product is fully TAA (Trade Agreement Act) compliant, making it suitable for institutional and clinical procurement requirements.
What are the dimensions of this size 3 ring?
The Size 3 model features a diameter of 2-1/2 inches, designed to provide appropriate support and fit for specific patient anatomy.
Is the material durable for its purpose?
The pessary is constructed from high-quality, medical-grade molded material. Its design is purposeful, ensuring both durability and ease of cleaning for clinical utility.
Does this include a support structure?
Yes, this is a ring-style pessary with support. The design incorporates a solid outer ring connected to a central structural plate featuring four apertures for functional stability.
Is this product considered a non-sterile device?
Yes, the device is categorized as a non-sterile surgical instrument. Medical professionals should follow established clinical protocols for sterilization and application before use.
What is the official HCPCS code for this device?
The official HCPCS code for this Integra Miltex Ring Pessary is A4562.
Is this device brand new from the factory?
Yes, all units provided are Factory New, ensuring they arrive in optimal condition for clinical use.
How should this professional instrument be utilized?
This pessary is intended exclusively for clinical use by medical professionals. It should be utilized in accordance with professional medical guidance and established clinical protocols for the management of pelvic organ prolapse.