PLASTOSILK (UDI 05900516896546)
Manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
Device Regulatory Overview
The PLASTOSILK (Model/Catalog Number: MA-162-MMMM-013) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MA-162-MMMM-013
- Product Code / EMDN
- M050101
- Device Name
- PLASTERS, ADHESIVE TAPES NON STERILE
- Database Sync Date
- 2026-08-09 16:30:34
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 PLASTOSILK?
The registered manufacturer of record for PLASTOSILK is TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for PLASTOSILK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516896546.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
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