eudamed_udi
Primary ID: 08903175001471
Paramount (UDI 08903175001471)
Manufactured by Paramount Surgimed Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Paramount - Primary ID 08903175001471
Device Regulatory Overview
The Paramount (Model/Catalog Number: PDSS19) is a medical device manufactured by Paramount Surgimed Limited. This product is indexed under FDA Product Code / Category Classification V010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PDSS19
- Product Code / EMDN
- V010102
- Device Name
- Disposable scalpel with or without safety features
- Database Sync Date
- 2026-08-09 16:50:49
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 Paramount?
The registered manufacturer of record for Paramount is Paramount Surgimed Limited.
What is the Primary UDI-DI identifier for Paramount?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08903175001471.
What classification code is assigned to this device?
This device is registered under product classification code V010102.
Similar Classification Devices (V010102)
Other Devices by Paramount Surgimed Limited
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