Nordent Manufacturing, Inc. (UDI 00840018640986)
Manufactured by Nordent Manufacturing Inc.
Device Regulatory Overview
The Nordent Manufacturing, Inc. (Model/Catalog Number: Nordent Surgery Catalogue) is a medical device manufactured by Nordent Manufacturing Inc.. This product is indexed under FDA Product Code / Category Classification L01040299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Nordent Surgery Catalogue
- Product Code / EMDN
- L01040299
- Device Name
- SCIS #302 CRVD 4-1/2/115MM
- Database Sync Date
- 2026-08-09 16:58:15
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 Nordent Manufacturing, Inc.?
The registered manufacturer of record for Nordent Manufacturing, Inc. is Nordent Manufacturing Inc..
What is the Primary UDI-DI identifier for Nordent Manufacturing, Inc.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840018640986.
What classification code is assigned to this device?
This device is registered under product classification code L01040299.
Similar Classification Devices (L01040299)
Other Devices by Nordent Manufacturing Inc.
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