eudamed_udi
Primary ID: 08681285119780
Bandiko (UDI 08681285119780)
Manufactured by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bandiko - Primary ID 08681285119780
Device Regulatory Overview
The Bandiko (Model/Catalog Number: BEN831) is a medical device manufactured by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş. This product is indexed under FDA Product Code / Category Classification M0599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BEN831
- Product Code / EMDN
- M0599
- Device Name
- Aid Plaster
- Database Sync Date
- 2026-08-09 16:46:39
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 Bandiko?
The registered manufacturer of record for Bandiko is Honnes Sağlık ve Endüstriyel Ürünleri A.Ş.
What is the Primary UDI-DI identifier for Bandiko?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681285119780.
What classification code is assigned to this device?
This device is registered under product classification code M0599.
Similar Classification Devices (M0599)
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