ERTRIAGE (UDI 05214003361128)
Manufactured by SINDROMITIKES IPIRESIES FRONTIDAS IGEIAS KAI TILEIATRIKIS IKE
Device Regulatory Overview
The ERTRIAGE (Model/Catalog Number: ERTRIAGE) is a medical device manufactured by SINDROMITIKES IPIRESIES FRONTIDAS IGEIAS KAI TILEIATRIKIS IKE. This product is indexed under FDA Product Code / Category Classification Z12030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ERTRIAGE
- Product Code / EMDN
- Z12030201
- Device Name
- ERTRIAGE
- Database Sync Date
- 2026-08-09 17:58:43
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 ERTRIAGE?
The registered manufacturer of record for ERTRIAGE is SINDROMITIKES IPIRESIES FRONTIDAS IGEIAS KAI TILEIATRIKIS IKE.
What is the Primary UDI-DI identifier for ERTRIAGE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05214003361128.
What classification code is assigned to this device?
This device is registered under product classification code Z12030201.
Similar Classification Devices (Z12030201)
Other Devices by SINDROMITIKES IPIRESIES FRONTIDAS IGEIAS KAI TILEIATRIKIS IKE
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