gudid
Primary ID: 310.572
NA (UDI 310.572)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID 310.572
Device Regulatory Overview
The NA (Model/Catalog Number: 310.572) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification HSZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 310.572
- Product Code / EMDN
- HSZ
- Device Name
- 2.4MM DRILL BIT STRYKER J-LATCH/75MM
- Database Sync Date
- 2026-08-09 09:39:08
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 Synthes GmbH.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 310.572.
What classification code is assigned to this device?
This device is registered under product classification code HSZ.
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