BOM (UDI 05900516501105)
Manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
Device Regulatory Overview
The BOM (Model/Catalog Number: OM-191-FPSA-026) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification S01010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OM-191-FPSA-026
- Product Code / EMDN
- S01010101
- Device Name
- MEDICAL PACKAGING
- Database Sync Date
- 2026-08-09 16:29:47
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BOM?
The registered manufacturer of record for BOM is TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA.
What is the Primary UDI-DI identifier for BOM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516501105.
What classification code is assigned to this device?
This device is registered under product classification code S01010101.
Similar Classification Devices (S01010101)
Other Devices by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint