gudid
Primary ID: 12012012
3M (UDI 12012012)
Manufactured by 3M Deutschland GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 3M - Primary ID 12012012
Device Regulatory Overview
The 3M (Model/Catalog Number: 12012012) is a medical device manufactured by 3M Deutschland GmbH. This product is indexed under FDA Product Code / Category Classification QGO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12012012
- Product Code / EMDN
- QGO
- Device Name
- 3M Filtek Composite Warmer
- Database Sync Date
- 2026-08-09 09:38:00
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 Deutschland GmbH.
What is the Primary UDI-DI identifier for 3M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12012012.
What classification code is assigned to this device?
This device is registered under product classification code QGO.
Similar Classification Devices (QGO)
Other Devices by 3M Deutschland GmbH
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