MATOLAST (UDI 05900516860776)
Manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
Device Regulatory Overview
The MATOLAST (Model/Catalog Number: MA-123-LA40-029) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification M0304010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MA-123-LA40-029
- Product Code / EMDN
- M0304010103
- Device Name
- BANDAGES NON STERILE
- Database Sync Date
- 2026-08-09 16:59:22
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 MATOLAST?
The registered manufacturer of record for MATOLAST is TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for MATOLAST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516860776.
What classification code is assigned to this device?
This device is registered under product classification code M0304010103.
Similar Classification Devices (M0304010103)
Other Devices by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
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