Descriptra

מחולל תיאורי ציוד רפואי בינה מלאכותית

צור תיאורים מדויקים ותואמי רגולציה לציוד רפואי. הדגש מידע קליני, שימוש ותקני בטיחות.

תואם רגולציה
מידע קליני
תקני בטיחות
Medical Device

Blood Pressure Monitor

FDA 510(k) Cleared

Bluetooth 5.0
Clinically Validated
2-User Memory

תכונות

FDA cleared ✓
CE marked ✓
ISO 13485 ✓

Regulatory Language

AI uses compliant phrasing: "intended for," "indicated for use in" — avoiding unapproved medical claims while remaining informative.

Class II
Clearance 510(k)
Standard IEC 62133

Technical Specifications

Accurately presents dimensions, materials, sterilization methods, power requirements, and certification numbers.

FDACEISOIECHIPAA

Certification Highlighting

Prominently displays FDA clearance, CE marking, ISO 13485, and other medical device certifications.

Compliance Score 97/100

Healthcare Professional Tone

Professional, clinical language that builds trust with healthcare buyers and procurement departments.

איך זה עובד

1

Enter Device Details

Product name, intended use, specifications, certifications, and contraindications.

2

Set Compliance Level

Class I, II, or III device. AI applies appropriate regulatory language depth.

3

Generate Description

Get compliant, professional descriptions with certification callouts.

ראה בפעולה

Medical Device

Input

Digital blood pressure monitor — upper arm, FDA cleared, Bluetooth, memory for 2 users, irregular heartbeat detection

Output

FDA-Cleared Digital Blood Pressure Monitor This clinically validated upper-arm blood pressure monitor provides accurate systolic, diastolic, and pulse readings for home health monitoring. Bluetooth connectivity syncs data to your smartphone for easy tracking. Dual-user memory stores up to 120 readings per user. Irregular heartbeat detection alerts you to potential arrhythmias during measurement. FDA 510(k) Cleared | Clinically Validated | Bluetooth 5.0

שאלות נפוצות

Does it follow FDA language guidelines?

Yes. AI uses compliant structure/function language and avoids unapproved medical claims.

Can it handle Class I, II, and III devices?

Yes. Regulatory language depth adapts based on device classification.

Compliant Medical Device Descriptions

Generate regulatory-aware medical device copy. 5 free credits.