FDA UDI In Commercial Distribution 🇺🇸 United States

Guidewire

DI: 00885672101466 · Model: GW35180 · Oscor Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Guidewire
Primary DI
00885672101466
Version / Model
GW35180
Catalog Number
GW35180
Company Name
Oscor Inc.
Labeler DUNS
101835833
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-07
Public Version
1
Public Version Date
2023-09-15
Public Version Status
New
Public Device Record Key
c53d9a15-7601-470f-93e0-937b71ee0110

Device Description

Guidewire with PTFE coating

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
DQX Wire, guide, catheter

GMDN Terms

Code Name
58115 Peripheral vascular guidewire, manual

Identifiers

Type ID
Primary 00885672101466

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.035 Inch
Length 180 Centimeter