gudid
Primary ID: PED-400-35
PIPELINE (UDI PED-400-35)
Manufactured by Micro Therapeutics, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PIPELINE - Primary ID PED-400-35
Device Regulatory Overview
The PIPELINE (Model/Catalog Number: PED-400-35) is a medical device manufactured by Micro Therapeutics, Inc.. This product is indexed under FDA Product Code / Category Classification OUT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PED-400-35
- Product Code / EMDN
- OUT
- Device Name
- PED-400-35 PIPELINE FLEX 4.00MM X 35MM
- Database Sync Date
- 2026-08-09 09:33:17
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 PIPELINE?
The registered manufacturer of record for PIPELINE is Micro Therapeutics, Inc..
What is the Primary UDI-DI identifier for PIPELINE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PED-400-35.
What classification code is assigned to this device?
This device is registered under product classification code OUT.
Similar Classification Devices (OUT)
Other Devices by Micro Therapeutics, Inc.
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