eudamed_udi
Primary ID: 08056215740608
CURETTE GRACEY 11-12 TIPO RIGIDO (UDI 08056215740608)
Manufactured by MEDESY srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CURETTE GRACEY 11-12 TIPO RIGIDO - Primary ID 08056215740608
Device Regulatory Overview
The CURETTE GRACEY 11-12 TIPO RIGIDO (Model/Catalog Number: 628/11-12.HL8) is a medical device manufactured by MEDESY srl. This product is indexed under FDA Product Code / Category Classification L159001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 628/11-12.HL8
- Product Code / EMDN
- L159001
- Device Name
- STRUMENTI CHIRURGICI RIUTILIZZABILI
- Database Sync Date
- 2026-08-09 16:29:02
Full Regulatory Attributes
🔒 Token Gated
{
"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 CURETTE GRACEY 11-12 TIPO RIGIDO?
The registered manufacturer of record for CURETTE GRACEY 11-12 TIPO RIGIDO is MEDESY srl.
What is the Primary UDI-DI identifier for CURETTE GRACEY 11-12 TIPO RIGIDO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056215740608.
What classification code is assigned to this device?
This device is registered under product classification code L159001.
Similar Classification Devices (L159001)
Other Devices by MEDESY srl
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