TUBILAST G LATEX FREE (UDI 06192491100162)
Manufactured by Plastic Electromechanic Company Medical International
Device Regulatory Overview
The TUBILAST G LATEX FREE (Model/Catalog Number: 106000207-10LF) is a medical device manufactured by Plastic Electromechanic Company Medical International. This product is indexed under FDA Product Code / Category Classification M0304010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 106000207-10LF
- Product Code / EMDN
- M0304010103
- Device Name
- TUBILAST
- Database Sync Date
- 2026-08-09 16:59:58
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 TUBILAST G LATEX FREE?
The registered manufacturer of record for TUBILAST G LATEX FREE is Plastic Electromechanic Company Medical International.
What is the Primary UDI-DI identifier for TUBILAST G LATEX FREE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06192491100162.
What classification code is assigned to this device?
This device is registered under product classification code M0304010103.
Similar Classification Devices (M0304010103)
Other Devices by Plastic Electromechanic Company Medical International
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