eudamed_udi
Primary ID: 06222023898233
Neoplast® latex free (UDI 06222023898233)
Manufactured by Pharmaplast
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neoplast® latex free - Primary ID 06222023898233
Device Regulatory Overview
The Neoplast® latex free (Model/Catalog Number: NEOLF1004000P) 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
- NEOLF1004000P
- Product Code / EMDN
- M050101
- Device Name
- Adhesive Tapes
- Database Sync Date
- 2026-08-09 16:29:00
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® latex free?
The registered manufacturer of record for Neoplast® latex free is Pharmaplast.
What is the Primary UDI-DI identifier for Neoplast® latex free?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06222023898233.
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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