FDA UDI In Commercial Distribution 🇺🇸 United States

ACCEL®

DI: 04046955639298 · Model: 613942 · B BRAUN INTERVENTIONAL SYSTEMS, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

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Basic Information

Brand Name
ACCEL®
Primary DI
04046955639298
Version / Model
613942
Catalog Number
613942
Company Name
B BRAUN INTERVENTIONAL SYSTEMS, INC
Labeler DUNS
784259751
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2024-05-12
Public Version
2
Public Version Date
2025-11-20
Public Version Status
Update
Public Device Record Key
58988e22-2e07-4394-902a-e7730fe62679

Device Description

ACCEL SECUREMENT DEVICE 5-12F

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KMK DEVICE, INTRAVASCULAR CATHETER SECUREMENT

GMDN Terms

Code Name
56631 Wearable percutaneous catheter/tube holder, single-use

Identifiers

Type ID
Unit of Use 04046955639281
Primary 04046955639298

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius