eudamed_udi
Primary ID: 06223003736378
Airoplast® (UDI 06223003736378)
Manufactured by Pharmaplast
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Airoplast® - Primary ID 06223003736378
Device Regulatory Overview
The Airoplast® (Model/Catalog Number: AIRO759140N) 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
- AIRO759140N
- Product Code / EMDN
- M050101
- Device Name
- Adhesive Tapes
- Database Sync Date
- 2026-08-09 16:30:30
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 Airoplast®?
The registered manufacturer of record for Airoplast® is Pharmaplast.
What is the Primary UDI-DI identifier for Airoplast®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06223003736378.
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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