FDA UDI In Commercial Distribution 🇺🇸 United States

ANGIOGUARD

DI: 10705032054782 · Model: 501814REC · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ANGIOGUARD
Primary DI
10705032054782
Version / Model
501814REC
Catalog Number
501814REC
Company Name
CORDIS CORPORATION
Labeler DUNS
806136177
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-26
Public Version
3
Public Version Date
2022-02-28
Public Version Status
Update
Public Device Record Key
5596daa0-637e-4478-838e-985ebae4dc52

Device Description

5MM BASKET, EXTRA SUPPORT,

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NTE Temporary Carotid Catheter for Embolic Capture

GMDN Terms

Code Name
44841 Embolic protection filtering guidewire

Identifiers

Type ID
Package 20705032054789
Primary 10705032054782