gudid
Primary ID: DMT4786
CVS (UDI DMT4786)
Manufactured by WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CVS - Primary ID DMT4786
Device Regulatory Overview
The CVS (Model/Catalog Number: DMT4786) is a medical device manufactured by WOONSOCKET PRESCRIPTION CENTER, INCORPORATED. This product is indexed under FDA Product Code / Category Classification SDV within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DMT4786
- Product Code / EMDN
- SDV
- Device Name
- A hand-held battery-powered, electronic instrument designed to measure a patient's body temperature. The device has a flexible tip and an LCD display. It is designed to take a temperature reading in approximately 5 seconds. This is a reusable device.
- Database Sync Date
- 2026-08-09 09:08:49
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 CVS?
The registered manufacturer of record for CVS is WOONSOCKET PRESCRIPTION CENTER, INCORPORATED.
What is the Primary UDI-DI identifier for CVS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DMT4786.
What classification code is assigned to this device?
This device is registered under product classification code SDV.
Similar Classification Devices (SDV)
Other Devices by WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint