gudid
Primary ID: 9166017V
Injekt (UDI 9166017V)
Manufactured by B. BRAUN MEDICAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Injekt - Primary ID 9166017V
Device Regulatory Overview
The Injekt (Model/Catalog Number: 9166017V) is a medical device manufactured by B. BRAUN MEDICAL INC.. This product is indexed under FDA Product Code / Category Classification FMF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9166017V
- Product Code / EMDN
- FMF
- Device Name
- Injekt-F (1 ml) (9166017V)
- Database Sync Date
- 2026-08-09 09:38:09
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 Injekt?
The registered manufacturer of record for Injekt is B. BRAUN MEDICAL INC..
What is the Primary UDI-DI identifier for Injekt?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9166017V.
What classification code is assigned to this device?
This device is registered under product classification code FMF.
Similar Classification Devices (FMF)
Other Devices by B. BRAUN MEDICAL INC.
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