eudamed_udi
Primary ID: 06943566100378
Y-Kelin® (UDI 06943566100378)
Manufactured by Anhui Greenland Biotech Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Y-Kelin® - Primary ID 06943566100378
Device Regulatory Overview
The Y-Kelin® (Model/Catalog Number: N/A) is a medical device manufactured by Anhui Greenland Biotech Co.,Ltd. This product is indexed under FDA Product Code / Category Classification Q010699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- Q010699
- Device Name
- Denture Adhesive Powder
- Database Sync Date
- 2026-08-09 16:28:45
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 Y-Kelin®?
The registered manufacturer of record for Y-Kelin® is Anhui Greenland Biotech Co.,Ltd.
What is the Primary UDI-DI identifier for Y-Kelin®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06943566100378.
What classification code is assigned to this device?
This device is registered under product classification code Q010699.
Similar Classification Devices (Q010699)
Other Devices by Anhui Greenland Biotech Co.,Ltd
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