GUDIDData
gudid Primary ID: LMT-RCT

Riptide Collection Canister with Intermediate Tubing (UDI LMT-RCT)

Manufactured by Micro Therapeutics, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Riptide Collection Canister with Intermediate Tubing - Primary ID LMT-RCT

Device Regulatory Overview

The Riptide Collection Canister with Intermediate Tubing (Model/Catalog Number: LMT-RCT) is a medical device manufactured by Micro Therapeutics, Inc.. This product is indexed under FDA Product Code / Category Classification JCX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
LMT-RCT
Product Code / EMDN
JCX
Device Name
CANISTER TUBING LMT-RCTV 02 LIBERANT
Database Sync Date
2026-08-09 09:41:30

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 Riptide Collection Canister with Intermediate Tubing?

The registered manufacturer of record for Riptide Collection Canister with Intermediate Tubing is Micro Therapeutics, Inc..

What is the Primary UDI-DI identifier for Riptide Collection Canister with Intermediate Tubing?

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

What classification code is assigned to this device?

This device is registered under product classification code JCX.

Programmatic Export

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

JSON API Endpoint