eudamed_udi
Primary ID: 06224000132613
Neoplast® (UDI 06224000132613)
Manufactured by Pharmaplast
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neoplast® - Primary ID 06224000132613
Device Regulatory Overview
The Neoplast® (Model/Catalog Number: NEO1005000P) is a medical device manufactured by Pharmaplast. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NEO1005000P
- Product Code / EMDN
- M050101
- Device Name
- Adhesive Tapes
- Database Sync Date
- 2026-08-09 16:29:06
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 Neoplast®?
The registered manufacturer of record for Neoplast® is Pharmaplast.
What is the Primary UDI-DI identifier for Neoplast®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06224000132613.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by Pharmaplast
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