gudid
Primary ID: 9667L
Solventum (UDI 9667L)
Manufactured by Solventum US LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Solventum - Primary ID 9667L
Device Regulatory Overview
The Solventum (Model/Catalog Number: 9667L) is a medical device manufactured by Solventum US LLC. This product is indexed under FDA Product Code / Category Classification LWK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9667L
- Product Code / EMDN
- LWK
- Device Name
- Solventum Surgical Clipper with Pivoting Head Starter Kit, 9667L, 9661LClipper and 9662L Charger Stand, 1 KIT/CS
- Database Sync Date
- 2026-08-09 09:18:30
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 Solventum?
The registered manufacturer of record for Solventum is Solventum US LLC.
What is the Primary UDI-DI identifier for Solventum?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9667L.
What classification code is assigned to this device?
This device is registered under product classification code LWK.
Similar Classification Devices (LWK)
Other Devices by Solventum US LLC
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