gudid
Primary ID: 1474R1
TMC38 (UDI 1474R1)
Manufactured by MEDTRONIC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TMC38 - Primary ID 1474R1
Device Regulatory Overview
The TMC38 (Model/Catalog Number: 1474R1) is a medical device manufactured by MEDTRONIC, INC.. This product is indexed under FDA Product Code / Category Classification DRY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1474R1
- Product Code / EMDN
- DRY
- Device Name
- CELL 1474R1 TMC38 W/6 EXTENSION
- Database Sync Date
- 2026-08-09 09:44:05
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 TMC38?
The registered manufacturer of record for TMC38 is MEDTRONIC, INC..
What is the Primary UDI-DI identifier for TMC38?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1474R1.
What classification code is assigned to this device?
This device is registered under product classification code DRY.
Similar Classification Devices (DRY)
Other Devices by MEDTRONIC, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint