gudid
Primary ID: 1
Remi Impression Kit (UDI 1)
Manufactured by GrindGuard Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Remi Impression Kit - Primary ID 1
Device Regulatory Overview
The Remi Impression Kit (Model/Catalog Number: 1) is a medical device manufactured by GrindGuard Inc.. This product is indexed under FDA Product Code / Category Classification SHI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- SHI
- Device Name
- Database Sync Date
- 2026-08-09 09:49:16
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 Remi Impression Kit?
The registered manufacturer of record for Remi Impression Kit is GrindGuard Inc..
What is the Primary UDI-DI identifier for Remi Impression Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code SHI.
Similar Classification Devices (SHI)
Other Devices by GrindGuard Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint