eudamed_udi
Primary ID: 08436630990107
Profilm Aphtes AR (10mL) (UDI 08436630990107)
Manufactured by i+Med S.Coop.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Profilm Aphtes AR (10mL) - Primary ID 08436630990107
Device Regulatory Overview
The Profilm Aphtes AR (10mL) (Model/Catalog Number: -) is a medical device manufactured by i+Med S.Coop.. This product is indexed under FDA Product Code / Category Classification M04040501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- -
- Product Code / EMDN
- M04040501
- Device Name
- Hidrogel para el tratamiento de heridas internas (AFTA1) / Hydrogel for the treatment of internal wounds (AFTA1)
- Database Sync Date
- 2026-08-09 16:47:35
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 Profilm Aphtes AR (10mL)?
The registered manufacturer of record for Profilm Aphtes AR (10mL) is i+Med S.Coop..
What is the Primary UDI-DI identifier for Profilm Aphtes AR (10mL)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436630990107.
What classification code is assigned to this device?
This device is registered under product classification code M04040501.
Similar Classification Devices (M04040501)
Other Devices by i+Med S.Coop.
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