gudid
Primary ID: 6177751
VITROS (UDI 6177751)
Manufactured by ORTHO CLINICAL DIAGNOSTICS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VITROS - Primary ID 6177751
Device Regulatory Overview
The VITROS (Model/Catalog Number: 6177751) is a medical device manufactured by ORTHO CLINICAL DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification LTK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6177751
- Product Code / EMDN
- LTK
- Device Name
- VITROS Immunodiagnostic Products CA 125 II Calibrators
- Database Sync Date
- 2026-08-09 10:00:16
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 VITROS?
The registered manufacturer of record for VITROS is ORTHO CLINICAL DIAGNOSTICS.
What is the Primary UDI-DI identifier for VITROS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6177751.
What classification code is assigned to this device?
This device is registered under product classification code LTK.
Similar Classification Devices (LTK)
Other Devices by ORTHO CLINICAL DIAGNOSTICS
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint