eudamed_udi
Primary ID: 06118002171018
PHARCOPLAST (UDI 06118002171018)
Manufactured by PHARCOMEDIC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PHARCOPLAST - Primary ID 06118002171018
Device Regulatory Overview
The PHARCOPLAST (Model/Catalog Number: 6118002171018) is a medical device manufactured by PHARCOMEDIC. This product is indexed under FDA Product Code / Category Classification M050202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6118002171018
- Product Code / EMDN
- M050202
- Device Name
- Perforated Adhesive tape
- Database Sync Date
- 2026-08-09 16:49:19
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 PHARCOPLAST?
The registered manufacturer of record for PHARCOPLAST is PHARCOMEDIC.
What is the Primary UDI-DI identifier for PHARCOPLAST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06118002171018.
What classification code is assigned to this device?
This device is registered under product classification code M050202.
Similar Classification Devices (M050202)
Other Devices by PHARCOMEDIC
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