gudid
Primary ID: 00600
Staclot LA (UDI 00600)
Manufactured by DIAGNOSTICA STAGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Staclot LA - Primary ID 00600
Device Regulatory Overview
The Staclot LA (Model/Catalog Number: 00600) is a medical device manufactured by DIAGNOSTICA STAGO. This product is indexed under FDA Product Code / Category Classification GFO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00600
- Product Code / EMDN
- GFO
- Device Name
- Database Sync Date
- 2026-08-09 09:23:29
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 Staclot LA?
The registered manufacturer of record for Staclot LA is DIAGNOSTICA STAGO.
What is the Primary UDI-DI identifier for Staclot LA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00600.
What classification code is assigned to this device?
This device is registered under product classification code GFO.
Similar Classification Devices (GFO)
Other Devices by DIAGNOSTICA STAGO
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