eudamed_udi
Primary ID: 04260748970287
PLASMO®HEAL PRO Applicator Tube (UDI 04260748970287)
Manufactured by WK-MedTec GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PLASMO®HEAL PRO Applicator Tube - Primary ID 04260748970287
Device Regulatory Overview
The PLASMO®HEAL PRO Applicator Tube (Model/Catalog Number: 3014) is a medical device manufactured by WK-MedTec GmbH. This product is indexed under FDA Product Code / Category Classification Z12019003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3014
- Product Code / EMDN
- Z12019003
- Device Name
- PLASMO®HEAL PRO Applicator
- Database Sync Date
- 2026-08-09 16:48:33
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 PLASMO®HEAL PRO Applicator Tube?
The registered manufacturer of record for PLASMO®HEAL PRO Applicator Tube is WK-MedTec GmbH.
What is the Primary UDI-DI identifier for PLASMO®HEAL PRO Applicator Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260748970287.
What classification code is assigned to this device?
This device is registered under product classification code Z12019003.
Similar Classification Devices (Z12019003)
Other Devices by WK-MedTec GmbH
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