gudid
Primary ID: DL-2000 P
Rexxam (UDI DL-2000 P)
Manufactured by REXXAM CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rexxam - Primary ID DL-2000 P
Device Regulatory Overview
The Rexxam (Model/Catalog Number: DL-2000 P) is a medical device manufactured by REXXAM CO., LTD.. This product is indexed under FDA Product Code / Category Classification HLM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DL-2000 P
- Product Code / EMDN
- HLM
- Device Name
- This device intends to measure vertex powers and prismatic effects of spectacle and contact lenses, to orientate and mark uncut lenses, and to verify the correct mounting of lenses in spectacle frames.
- Database Sync Date
- 2026-08-09 09:53:17
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 Rexxam?
The registered manufacturer of record for Rexxam is REXXAM CO., LTD..
What is the Primary UDI-DI identifier for Rexxam?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DL-2000 P.
What classification code is assigned to this device?
This device is registered under product classification code HLM.
Similar Classification Devices (HLM)
Other Devices by REXXAM CO., LTD.
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