TUBIFIX P1/2 (UDI 06192491100599)
Manufactured by Plastic Electromechanic Company Medical International
Device Regulatory Overview
The TUBIFIX P1/2 (Model/Catalog Number: 106000030-10) 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
- 106000030-10
- Product Code / EMDN
- M0303010103
- Device Name
- Tubifix
- Database Sync Date
- 2026-08-09 17:07:14
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 TUBIFIX P1/2?
The registered manufacturer of record for TUBIFIX P1/2 is Plastic Electromechanic Company Medical International.
What is the Primary UDI-DI identifier for TUBIFIX P1/2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06192491100599.
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
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