MATOSOFT SYNTHETIC (UDI 05900516890889)
Manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
Device Regulatory Overview
The MATOSOFT SYNTHETIC (Model/Catalog Number: MA-173-SYNT-008) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification M01020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MA-173-SYNT-008
- Product Code / EMDN
- M01020202
- Device Name
- ORTHOPAEDIC PADDINGS NON STERILE
- Database Sync Date
- 2026-08-09 16:29:06
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 MATOSOFT SYNTHETIC?
The registered manufacturer of record for MATOSOFT SYNTHETIC is TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for MATOSOFT SYNTHETIC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516890889.
What classification code is assigned to this device?
This device is registered under product classification code M01020202.
Similar Classification Devices (M01020202)
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