eudamed_udi
Primary ID: 04250108368083
Actolind w Gel 25x5 monodose tube ml (UDI 04250108368083)
Manufactured by ACTO GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Actolind w Gel 25x5 monodose tube ml - Primary ID 04250108368083
Device Regulatory Overview
The Actolind w Gel 25x5 monodose tube ml (Model/Catalog Number: 06.6803.05M25) is a medical device manufactured by ACTO GmbH. This product is indexed under FDA Product Code / Category Classification M040412 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 06.6803.05M25
- Product Code / EMDN
- M040412
- Device Name
- Wound Care Gel
- Database Sync Date
- 2026-08-09 16:28:58
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 Actolind w Gel 25x5 monodose tube ml?
The registered manufacturer of record for Actolind w Gel 25x5 monodose tube ml is ACTO GmbH.
What is the Primary UDI-DI identifier for Actolind w Gel 25x5 monodose tube ml?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250108368083.
What classification code is assigned to this device?
This device is registered under product classification code M040412.
Similar Classification Devices (M040412)
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