gudid
Primary ID: SR-6000
NA (UDI SR-6000)
Manufactured by MEDTRONIC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID SR-6000
Device Regulatory Overview
The NA (Model/Catalog Number: SR-6000) is a medical device manufactured by MEDTRONIC, INC.. This product is indexed under FDA Product Code / Category Classification GXR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SR-6000
- Product Code / EMDN
- GXR
- Device Name
- SCREW SR-6000 CRANIAL BONE 1.6X6MM 6PK
- Database Sync Date
- 2026-08-09 09:44:10
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 NA?
The registered manufacturer of record for NA is MEDTRONIC, INC..
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SR-6000.
What classification code is assigned to this device?
This device is registered under product classification code GXR.
Similar Classification Devices (GXR)
Other Devices by MEDTRONIC, INC.
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