eudamed_udi
Primary ID: 08058090006008
Bracciale Sfigmomanometro linea CHECK (UDI 08058090006008)
Manufactured by Pikdare S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bracciale Sfigmomanometro linea CHECK - Primary ID 08058090006008
Device Regulatory Overview
The Bracciale Sfigmomanometro linea CHECK (Model/Catalog Number: 02022013300000) is a medical device manufactured by Pikdare S.p.A.. This product is indexed under FDA Product Code / Category Classification Z1203020599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02022013300000
- Product Code / EMDN
- Z1203020599
- Device Name
- Bracciale Sfigmomanometro linea CHECK
- Database Sync Date
- 2026-08-09 16:29:48
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 Bracciale Sfigmomanometro linea CHECK?
The registered manufacturer of record for Bracciale Sfigmomanometro linea CHECK is Pikdare S.p.A..
What is the Primary UDI-DI identifier for Bracciale Sfigmomanometro linea CHECK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058090006008.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020599.
Similar Classification Devices (Z1203020599)
Other Devices by Pikdare S.p.A.
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