FDA UDI In Commercial Distribution 🇺🇸 United States

Wholey™

DI: 00763000185701 · Model: WWIJ35175 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Wholey™
Primary DI
00763000185701
Version / Model
WWIJ35175
Company Name
Covidien LP
Labeler DUNS
968903703
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-25
Public Version
2
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
3105c54d-aa9a-4102-b606-4ccc1ab7cbb9

Device Description

GW WWIJ35175 WHOLEY WIRE V04

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
No
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 20763000185705
Primary 00763000185701

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120863 000

Device Sizes

Type Value Unit Text
Guidewire Diameter 0.089 Centimeter
Guidewire Length 175.0 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store the guidewire away from sunlight at room temperature in a dry place.