GUDIDData
gudid Primary ID: KIT

Impression Kit Standard (UDI KIT)

Manufactured by STRAIGHT SMILE LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Impression Kit Standard - Primary ID KIT

Device Regulatory Overview

The Impression Kit Standard (Model/Catalog Number: KIT) is a medical device manufactured by STRAIGHT SMILE LLC. This product is indexed under FDA Product Code / Category Classification ELW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KIT
Product Code / EMDN
ELW
Device Name
Elastomeric Impression Material; Putty Base + Catalyst/Hand-mix (Type 0); Impression Kit
Database Sync Date
2026-08-09 09:37:45

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 Impression Kit Standard?

The registered manufacturer of record for Impression Kit Standard is STRAIGHT SMILE LLC.

What is the Primary UDI-DI identifier for Impression Kit Standard?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KIT.

What classification code is assigned to this device?

This device is registered under product classification code ELW.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint