gudid
Primary ID: 622287
ASEPT (UDI 622287)
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 ASEPT - Primary ID 622287
Device Regulatory Overview
The ASEPT (Model/Catalog Number: 622287) is a medical device manufactured by B BRAUN INTERVENTIONAL SYSTEMS, INC. This product is indexed under FDA Product Code / Category Classification DWM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 622287
- Product Code / EMDN
- DWM
- Device Name
- ASEPT 600ML DRAINAGE KIT
- Database Sync Date
- 2026-08-09 10:02:27
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 ASEPT?
The registered manufacturer of record for ASEPT is B BRAUN INTERVENTIONAL SYSTEMS, INC.
What is the Primary UDI-DI identifier for ASEPT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 622287.
What classification code is assigned to this device?
This device is registered under product classification code DWM.
Similar Classification Devices (DWM)
Other Devices by B BRAUN INTERVENTIONAL SYSTEMS, INC
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