Wellion PROTECT PRO SAFETY PENNEEDLES (UDI 09010727000543)
Manufactured by MED TRUST Handelsges.m.b.H.
Device Regulatory Overview
The Wellion PROTECT PRO SAFETY PENNEEDLES (Model/Catalog Number: WELL128R) is a medical device manufactured by MED TRUST Handelsges.m.b.H.. This product is indexed under FDA Product Code / Category Classification A0101010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WELL128R
- Product Code / EMDN
- A0101010201
- Device Name
- Wellion PROTECT PRO SAFETY PENNEEDLES
- Database Sync Date
- 2026-08-09 16:48:50
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 Wellion PROTECT PRO SAFETY PENNEEDLES?
The registered manufacturer of record for Wellion PROTECT PRO SAFETY PENNEEDLES is MED TRUST Handelsges.m.b.H..
What is the Primary UDI-DI identifier for Wellion PROTECT PRO SAFETY PENNEEDLES?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09010727000543.
What classification code is assigned to this device?
This device is registered under product classification code A0101010201.
Similar Classification Devices (A0101010201)
Other Devices by MED TRUST Handelsges.m.b.H.
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