CODOFIX (UDI 05900516278311)
Manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
Device Regulatory Overview
The CODOFIX (Model/Catalog Number: MA-123-CF10-003) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification M03030103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MA-123-CF10-003
- Product Code / EMDN
- M03030103
- Device Name
- ELASTIC DRESSING MESHES NON STERILE
- Database Sync Date
- 2026-08-09 16:49:21
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 CODOFIX?
The registered manufacturer of record for CODOFIX is TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for CODOFIX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516278311.
What classification code is assigned to this device?
This device is registered under product classification code M03030103.
Similar Classification Devices (M03030103)
Other Devices by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
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