eudamed_udi
Primary ID: 08058090054801
Ultimate V (UDI 08058090054801)
Manufactured by Pikdare S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ultimate V - Primary ID 08058090054801
Device Regulatory Overview
The Ultimate V (Model/Catalog Number: 81031830001000) is a medical device manufactured by Pikdare S.p.A.. This product is indexed under FDA Product Code / Category Classification A0101010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 81031830001000
- Product Code / EMDN
- A0101010202
- Device Name
- PEN NEEDLE
- Database Sync Date
- 2026-08-09 16:28:54
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 Ultimate V?
The registered manufacturer of record for Ultimate V is Pikdare S.p.A..
What is the Primary UDI-DI identifier for Ultimate V?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058090054801.
What classification code is assigned to this device?
This device is registered under product classification code A0101010202.
Similar Classification Devices (A0101010202)
Other Devices by Pikdare S.p.A.
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