GUDIDData
gudid Primary ID: 63312S

SML (UDI 63312S)

Manufactured by SELANE PRODUCTS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SML - Primary ID 63312S

Device Regulatory Overview

The SML (Model/Catalog Number: 63312S) is a medical device manufactured by SELANE PRODUCTS, INC.. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
63312S
Product Code / EMDN
LRK
Device Name
TAP/TALON
Database Sync Date
2026-08-09 09:03:36

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of SML?

The registered manufacturer of record for SML is SELANE PRODUCTS, INC..

What is the Primary UDI-DI identifier for SML?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 63312S.

What classification code is assigned to this device?

This device is registered under product classification code LRK.

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