SETON (UDI 05900516898793)
Manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
Device Regulatory Overview
The SETON (Model/Catalog Number: MA-105-MMMM-080) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification M0201050201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MA-105-MMMM-080
- Product Code / EMDN
- M0201050201
- Device Name
- DRESSING MATERIALS - SURGICALLY INVASIVE STERILE
- Database Sync Date
- 2026-08-09 16:28:48
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 SETON?
The registered manufacturer of record for SETON is TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for SETON?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516898793.
What classification code is assigned to this device?
This device is registered under product classification code M0201050201.
Similar Classification Devices (M0201050201)
Other Devices by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
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