inLink (UDI 03663394477062)

Manufactured by anthogyr

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The inLink (Model/Catalog Number: ILPCCR-4) is a medical device manufactured by anthogyr. This product is indexed under FDA Product Code / Category Classification Q010299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ILPCCR-4
Product Code / EMDN: Q010299
Device Name: Protection cap for lock
Database Sync Date: 2026-08-09 16:29:57

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 inLink?

The registered manufacturer of record for inLink is anthogyr.

What is the Primary UDI-DI identifier for inLink?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03663394477062.

What classification code is assigned to this device?

This device is registered under product classification code Q010299.

Similar Classification Devices (Q010299)

Other Devices by anthogyr

Programmatic Export

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

JSON API Endpoint