gudid
Primary ID: 614788
G-ARMOR STENT (UDI 614788)
Manufactured by B BRAUN INTERVENTIONAL SYSTEMS, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for G-ARMOR STENT - Primary ID 614788
Device Regulatory Overview
The G-ARMOR STENT (Model/Catalog Number: 614788) is a medical device manufactured by B BRAUN INTERVENTIONAL SYSTEMS, INC. This product is indexed under FDA Product Code / Category Classification PNF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 614788
- Product Code / EMDN
- PNF
- Device Name
- G ARMOR GM022 5.7cm 20mm 6cm 14F
- Database Sync Date
- 2026-08-09 09:43:17
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 G-ARMOR STENT?
The registered manufacturer of record for G-ARMOR STENT is B BRAUN INTERVENTIONAL SYSTEMS, INC.
What is the Primary UDI-DI identifier for G-ARMOR STENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 614788.
What classification code is assigned to this device?
This device is registered under product classification code PNF.
Similar Classification Devices (PNF)
Other Devices by B BRAUN INTERVENTIONAL SYSTEMS, INC
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