eudamed_udi
Primary ID: 80575070251752
STARK 19 (UDI 80575070251752)
Manufactured by NOI DELLA NOTTE SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STARK 19 - Primary ID 80575070251752
Device Regulatory Overview
The STARK 19 (Model/Catalog Number: 26PFRESTR - FS) is a medical device manufactured by NOI DELLA NOTTE SRL. This product is indexed under FDA Product Code / Category Classification V080699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 26PFRESTR - FS
- Product Code / EMDN
- V080699
- Device Name
- STARK 19 MATRIMONIALE
- Database Sync Date
- 2026-08-09 16:46:01
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 STARK 19?
The registered manufacturer of record for STARK 19 is NOI DELLA NOTTE SRL.
What is the Primary UDI-DI identifier for STARK 19?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80575070251752.
What classification code is assigned to this device?
This device is registered under product classification code V080699.
Similar Classification Devices (V080699)
Other Devices by NOI DELLA NOTTE SRL
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