AERO Fıx (UDI 08681285122049)
Manufactured by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş
Device Regulatory Overview
The AERO Fıx (Model/Catalog Number: AFR50) is a medical device manufactured by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş. This product is indexed under FDA Product Code / Category Classification M03030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AFR50
- Product Code / EMDN
- M03030199
- Device Name
- Medical Plaster
- Database Sync Date
- 2026-08-09 16:30:17
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of AERO Fıx?
The registered manufacturer of record for AERO Fıx is Honnes Sağlık ve Endüstriyel Ürünleri A.Ş.
What is the Primary UDI-DI identifier for AERO Fıx?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681285122049.
What classification code is assigned to this device?
This device is registered under product classification code M03030199.
Similar Classification Devices (M03030199)
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