FDA UDI In Commercial Distribution 🇺🇸 United States

Hi-Torque Proceed™

DI: 08717648321405 · Model: 1030903 · ABBOTT VASCULAR INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Hi-Torque Proceed™
Primary DI
08717648321405
Version / Model
1030903
Catalog Number
1030903
Company Name
ABBOTT VASCULAR INC.
Labeler DUNS
964569052
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-18
Public Version
2
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
dacb9ffd-ee9b-4aa0-9135-527f80f664ca

Device Description

Hi-Torque Proceed 220T Angled Guide Wire w/Hydrophilic Coating .014” 190 cm

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
Yes
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
DQX Wire, guide, catheter

GMDN Terms

Code Name
58115 Peripheral vascular guidewire, manual

Identifiers

Type ID
Package 28717648321409
Primary 08717648321405

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dry, dark, cool place.