gudid
Primary ID: E7003
Bausch + Lomb (UDI E7003)
Manufactured by Bausch & Lomb Incorporated
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bausch + Lomb - Primary ID E7003
Device Regulatory Overview
The Bausch + Lomb (Model/Catalog Number: E7003) is a medical device manufactured by Bausch & Lomb Incorporated. This product is indexed under FDA Product Code / Category Classification HRB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E7003
- Product Code / EMDN
- HRB
- Device Name
- OSHER HD MAGNIFIER
- Database Sync Date
- 2026-08-09 09:44:11
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 Bausch + Lomb?
The registered manufacturer of record for Bausch + Lomb is Bausch & Lomb Incorporated.
What is the Primary UDI-DI identifier for Bausch + Lomb?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E7003.
What classification code is assigned to this device?
This device is registered under product classification code HRB.
Similar Classification Devices (HRB)
Other Devices by Bausch & Lomb Incorporated
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint