eudamed_udi
Primary ID: 04571607489544
JM475BL015719 (UDI 04571607489544)
Manufactured by JAPAN OPTICAL CO.,LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for JM475BL015719 - Primary ID 04571607489544
Device Regulatory Overview
The JM475BL015719 (Model/Catalog Number: KIT209) is a medical device manufactured by JAPAN OPTICAL CO.,LTD.. This product is indexed under FDA Product Code / Category Classification Q02100203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KIT209
- Product Code / EMDN
- Q02100203
- Device Name
- SPECTACLE FRAMES - Full rim - Mixed
- Database Sync Date
- 2026-08-09 16:28:58
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 JM475BL015719?
The registered manufacturer of record for JM475BL015719 is JAPAN OPTICAL CO.,LTD..
What is the Primary UDI-DI identifier for JM475BL015719?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04571607489544.
What classification code is assigned to this device?
This device is registered under product classification code Q02100203.
Similar Classification Devices (Q02100203)
Other Devices by JAPAN OPTICAL CO.,LTD.
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