gudid
Primary ID: 102
Restoration (UDI 102)
Manufactured by ACESO DENTAL LABORATORY COMPANY LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Restoration - Primary ID 102
Device Regulatory Overview
The Restoration (Model/Catalog Number: 102) is a medical device manufactured by ACESO DENTAL LABORATORY COMPANY LIMITED. This product is indexed under FDA Product Code / Category Classification NSL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 102
- Product Code / EMDN
- NSL
- Device Name
- Database Sync Date
- 2026-08-09 09:06:41
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 Restoration?
The registered manufacturer of record for Restoration is ACESO DENTAL LABORATORY COMPANY LIMITED.
What is the Primary UDI-DI identifier for Restoration?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 102.
What classification code is assigned to this device?
This device is registered under product classification code NSL.
Similar Classification Devices (NSL)
Other Devices by ACESO DENTAL LABORATORY COMPANY LIMITED
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