eudamed_udi
Primary ID: 08051277605988
GUANCIALE LAB BACK&SIDE 9 CE (UDI 08051277605988)
Manufactured by TECHNOGEL ITALIA SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GUANCIALE LAB BACK&SIDE 9 CE - Primary ID 08051277605988
Device Regulatory Overview
The GUANCIALE LAB BACK&SIDE 9 CE (Model/Catalog Number: TG-PIL1B09CE) is a medical device manufactured by TECHNOGEL ITALIA SRL. This product is indexed under FDA Product Code / Category Classification V080399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TG-PIL1B09CE
- Product Code / EMDN
- V080399
- Device Name
- LAB BACK&SIDE
- Database Sync Date
- 2026-08-09 16:46:06
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 GUANCIALE LAB BACK&SIDE 9 CE?
The registered manufacturer of record for GUANCIALE LAB BACK&SIDE 9 CE is TECHNOGEL ITALIA SRL.
What is the Primary UDI-DI identifier for GUANCIALE LAB BACK&SIDE 9 CE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051277605988.
What classification code is assigned to this device?
This device is registered under product classification code V080399.
Similar Classification Devices (V080399)
Other Devices by TECHNOGEL ITALIA SRL
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