gudid
Primary ID: 0600-2110-000
Filter Line (UDI 0600-2110-000)
Manufactured by MECTRA LABS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Filter Line - Primary ID 0600-2110-000
Device Regulatory Overview
The Filter Line (Model/Catalog Number: 0600-2110-000) is a medical device manufactured by MECTRA LABS, INC.. This product is indexed under FDA Product Code / Category Classification HIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0600-2110-000
- Product Code / EMDN
- HIF
- Device Name
- Filter Line Luer Connector
- Database Sync Date
- 2026-08-09 09:32:55
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 Filter Line?
The registered manufacturer of record for Filter Line is MECTRA LABS, INC..
What is the Primary UDI-DI identifier for Filter Line?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0600-2110-000.
What classification code is assigned to this device?
This device is registered under product classification code HIF.
Similar Classification Devices (HIF)
Other Devices by MECTRA LABS, INC.
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