gudid
Primary ID: A
Securement Device (UDI A)
Manufactured by TILLA CARE LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Securement Device - Primary ID A
Device Regulatory Overview
The Securement Device (Model/Catalog Number: A) is a medical device manufactured by TILLA CARE LTD. This product is indexed under FDA Product Code / Category Classification NZU within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A
- Product Code / EMDN
- NZU
- Device Name
- Product GMCSD1001 , manufacture for Greystone medical
- Database Sync Date
- 2026-08-09 09:18:13
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 Securement Device?
The registered manufacturer of record for Securement Device is TILLA CARE LTD.
What is the Primary UDI-DI identifier for Securement Device?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A.
What classification code is assigned to this device?
This device is registered under product classification code NZU.
Similar Classification Devices (NZU)
Other Devices by TILLA CARE LTD
Programmatic Export
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