Alpheta (UDI 08681285101570)
Manufactured by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş
Device Regulatory Overview
The Alpheta (Model/Catalog Number: A7905) 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
- A7905
- Product Code / EMDN
- M03030199
- Device Name
- Kinesio Tape
- Database Sync Date
- 2026-08-09 16:49:20
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 Alpheta?
The registered manufacturer of record for Alpheta is Honnes Sağlık ve Endüstriyel Ürünleri A.Ş.
What is the Primary UDI-DI identifier for Alpheta?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681285101570.
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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