gudid
Primary ID: 010
SA-18 (UDI 010)
Manufactured by LAGADO CORPORATION, THE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SA-18 - Primary ID 010
Device Regulatory Overview
The SA-18 (Model/Catalog Number: 010) is a medical device manufactured by LAGADO CORPORATION, THE. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 010
- Product Code / EMDN
- HQD
- Device Name
- SA-18 Silicone Acrylate daily wear contact lens
- Database Sync Date
- 2026-08-09 09:49:26
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 SA-18?
The registered manufacturer of record for SA-18 is LAGADO CORPORATION, THE.
What is the Primary UDI-DI identifier for SA-18?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 010.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
Other Devices by LAGADO CORPORATION, THE
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