SENI ACTIVE SUPER (UDI 05900516695774)
Manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
Device Regulatory Overview
The SENI ACTIVE SUPER (Model/Catalog Number: SE-096-XL10-AD1) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification T04010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SE-096-XL10-AD1
- Product Code / EMDN
- T04010103
- Device Name
- ELASTIC DISPOSABLE UNDERWEAR
- Database Sync Date
- 2026-08-09 16:29:35
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 SENI ACTIVE SUPER?
The registered manufacturer of record for SENI ACTIVE SUPER is TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for SENI ACTIVE SUPER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516695774.
What classification code is assigned to this device?
This device is registered under product classification code T04010103.
Similar Classification Devices (T04010103)
Other Devices by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
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