gudid
Primary ID: MD300C205
CVS (UDI MD300C205)
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 MD300C205
Device Regulatory Overview
The CVS (Model/Catalog Number: MD300C205) is a medical device manufactured by WOONSOCKET PRESCRIPTION CENTER, INCORPORATED. This product is indexed under FDA Product Code / Category Classification PGJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MD300C205
- Product Code / EMDN
- PGJ
- Device Name
- CVS PULSE OXIMETER
- Database Sync Date
- 2026-08-09 09:08:49
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 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 MD300C205.
What classification code is assigned to this device?
This device is registered under product classification code PGJ.
Similar Classification Devices (PGJ)
Other Devices by WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
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