FDA UDI In Commercial Distribution 🇺🇸 United States

AVX

DI: 00616258003832 · Model: 105039-001 · Bayer Healthcare LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
AVX
Primary DI
00616258003832
Version / Model
105039-001
Catalog Number
105039
Company Name
Bayer Healthcare LLC
Labeler DUNS
079415074
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-10-09
Public Version
4
Public Version Date
2022-11-09
Public Version Status
Update
Public Device Record Key
b2964cfc-0eb1-4f6b-b46f-fcd0ee4624b8

Device Description

AVX CUS CATHETER, FG PKG

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DXE Catheter, Embolectomy

GMDN Terms

Code Name
58173 Thrombectomy suction catheter

Identifiers

Type ID
Primary 00616258003832

Customer Contacts

Phone
763-780-4555

Device Sizes

Type Value Unit Text
Catheter Gauge 6 French