gudid
Primary ID: 9681
3M (UDI 9681)
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 9681
Device Regulatory Overview
The 3M (Model/Catalog Number: 9681) 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
- 9681
- Product Code / EMDN
- LWK
- Device Name
- 3M Surgical Clipper Professional, 9681, 1/CV
- Database Sync Date
- 2026-08-09 09:04:14
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)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 9681.
What classification code is assigned to this device?
This device is registered under product classification code LWK.
Similar Classification Devices (LWK)
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