GUDIDData
gudid Primary ID: TIK0001L

Target Endoscopic Instrument (UDI TIK0001L)

Manufactured by SOLENDOS Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Target Endoscopic Instrument - Primary ID TIK0001L

Device Regulatory Overview

The Target Endoscopic Instrument (Model/Catalog Number: TIK0001L) is a medical device manufactured by SOLENDOS Inc.. This product is indexed under FDA Product Code / Category Classification HTS within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TIK0001L
Product Code / EMDN
HTS
Device Name
[Target] TIK0001L Indian Knife(Long)
Database Sync Date
2026-08-09 09:09:01

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 Target Endoscopic Instrument?

The registered manufacturer of record for Target Endoscopic Instrument is SOLENDOS Inc..

What is the Primary UDI-DI identifier for Target Endoscopic Instrument?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TIK0001L.

What classification code is assigned to this device?

This device is registered under product classification code HTS.

Programmatic Export

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

JSON API Endpoint