Blue EF Series,Splint (UDI 182)
Manufactured by Modern Dental Laboratory (DG) Co., Ltd.
Device Regulatory Overview
The Blue EF Series,Splint (Model/Catalog Number: 182) is a medical device manufactured by Modern Dental Laboratory (DG) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 182
- Product Code / EMDN
- LRK
- Device Name
- Database Sync Date
- 2026-08-09 09:06:41
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Blue EF Series,Splint?
The registered manufacturer of record for Blue EF Series,Splint is Modern Dental Laboratory (DG) Co., Ltd..
What is the Primary UDI-DI identifier for Blue EF Series,Splint?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 182.
What classification code is assigned to this device?
This device is registered under product classification code LRK.
Similar Classification Devices (LRK)
Other Devices by Modern Dental Laboratory (DG) Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint