Pansement sparadrap microporeux renforcé NEO‐STERILE‐STRIPS® 6mmx7.5cm (UDI D-F19306WD)
Manufactured by Adhe-Els SA.
Device Regulatory Overview
The Pansement sparadrap microporeux renforcé NEO‐STERILE‐STRIPS® 6mmx7.5cm (Model/Catalog Number: F19306) is a medical device manufactured by Adhe-Els SA.. This product is indexed under FDA Product Code / Category Classification M04010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F19306
- Product Code / EMDN
- M04010201
- Device Name
- Pansement sparadrap microporeux renforcé NEO‐STERILE‐STRIPS® 6mmx7.5cm
- Database Sync Date
- 2026-08-09 16:29:16
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 Pansement sparadrap microporeux renforcé NEO‐STERILE‐STRIPS® 6mmx7.5cm?
The registered manufacturer of record for Pansement sparadrap microporeux renforcé NEO‐STERILE‐STRIPS® 6mmx7.5cm is Adhe-Els SA..
What is the Primary UDI-DI identifier for Pansement sparadrap microporeux renforcé NEO‐STERILE‐STRIPS® 6mmx7.5cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-F19306WD.
What classification code is assigned to this device?
This device is registered under product classification code M04010201.
Similar Classification Devices (M04010201)
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