Plasmafit® (UDI 04046964115806)
Manufactured by Aesculap AG
Device Regulatory Overview
The Plasmafit® (Model/Catalog Number: NV001T) is a medical device manufactured by Aesculap AG. This product is indexed under FDA Product Code / Category Classification P090803010299 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R....
AESCULAP ELAN 4 FIXED DURAGUARD LONG. Model Number: GB943R....
Technical Specifications
- Model Number
- NV001T
- Product Code / EMDN
- P090803010299
- Device Name
- Acetabular cup closing screw
- Database Sync Date
- 2026-08-09 17:38:49
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 Plasmafit®?
The registered manufacturer of record for Plasmafit® is Aesculap AG.
What is the Primary UDI-DI identifier for Plasmafit®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046964115806.
What classification code is assigned to this device?
This device is registered under product classification code P090803010299.
Similar Classification Devices (P090803010299)
Other Devices by Aesculap AG
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