GUDIDData
gudid Primary ID: 9667L-A

3M (UDI 9667L-A)

Manufactured by 3M COMPANY

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 3M - Primary ID 9667L-A

Device Regulatory Overview

The 3M (Model/Catalog Number: 9667L-A) is a medical device manufactured by 3M COMPANY. This product is indexed under FDA Product Code / Category Classification LWK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
9667L-A
Product Code / EMDN
LWK
Device Name
3M Surgical Clipper Starter Kit (9661L Clipper and 9663L Charger Stand) 9667L-A
Database Sync Date
2026-08-09 10:00:20

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 3M?

The registered manufacturer of record for 3M is 3M COMPANY.

What is the Primary UDI-DI identifier for 3M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9667L-A.

What classification code is assigned to this device?

This device is registered under product classification code LWK.

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