gudid
Primary ID: TBD
ScleralFil (UDI TBD)
Manufactured by Bausch & Lomb Incorporated
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ScleralFil - Primary ID TBD
Device Regulatory Overview
The ScleralFil (Model/Catalog Number: TBD) is a medical device manufactured by Bausch & Lomb Incorporated. This product is indexed under FDA Product Code / Category Classification MRC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TBD
- Product Code / EMDN
- MRC
- Device Name
- Contact Lens Sterile Saline Solution
- Database Sync Date
- 2026-08-09 09:20:12
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 ScleralFil?
The registered manufacturer of record for ScleralFil is Bausch & Lomb Incorporated.
What is the Primary UDI-DI identifier for ScleralFil?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TBD.
What classification code is assigned to this device?
This device is registered under product classification code MRC.
Similar Classification Devices (MRC)
Other Devices by Bausch & Lomb Incorporated
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint