TUBIFIX S8 LATEX FREE (UDI 06192491100094)
Manufactured by Plastic Electromechanic Company Medical International
Device Regulatory Overview
The TUBIFIX S8 LATEX FREE (Model/Catalog Number: 106000028-10LF) is a medical device manufactured by Plastic Electromechanic Company Medical International. This product is indexed under FDA Product Code / Category Classification M0303010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 106000028-10LF
- Product Code / EMDN
- M0303010103
- Device Name
- Tubifix
- Database Sync Date
- 2026-08-09 17:27:11
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 TUBIFIX S8 LATEX FREE?
The registered manufacturer of record for TUBIFIX S8 LATEX FREE is Plastic Electromechanic Company Medical International.
What is the Primary UDI-DI identifier for TUBIFIX S8 LATEX FREE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06192491100094.
What classification code is assigned to this device?
This device is registered under product classification code M0303010103.
Similar Classification Devices (M0303010103)
Other Devices by Plastic Electromechanic Company Medical International
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint