eudamed_udi
Primary ID: 08058090051183
CEROTTO SU ROCCHETTO IN TELA (UDI 08058090051183)
Manufactured by Pikdare S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CEROTTO SU ROCCHETTO IN TELA - Primary ID 08058090051183
Device Regulatory Overview
The CEROTTO SU ROCCHETTO IN TELA (Model/Catalog Number: 58083581000000) is a medical device manufactured by Pikdare S.p.A.. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 58083581000000
- Product Code / EMDN
- M050101
- Device Name
- CEROTTO SU ROCCHETTO IN TELA
- Database Sync Date
- 2026-08-09 16:29:41
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 CEROTTO SU ROCCHETTO IN TELA?
The registered manufacturer of record for CEROTTO SU ROCCHETTO IN TELA is Pikdare S.p.A..
What is the Primary UDI-DI identifier for CEROTTO SU ROCCHETTO IN TELA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058090051183.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by Pikdare S.p.A.
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