FDA UDI In Commercial Distribution 🇺🇸 United States

Starter™ Guidewire

DI: 08714729326830 · Model: M001491751 · LAKE REGION MEDICAL LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Starter™ Guidewire
Primary DI
08714729326830
Version / Model
M001491751
Catalog Number
49-175
Company Name
LAKE REGION MEDICAL LIMITED
Labeler DUNS
988555595
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-07
Public Version
3
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
69d77a1b-e82b-4c95-a155-caa6364b3e2e

Device Description

Bentson Guidewire

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
Package 08714729743392
Primary 08714729326830

Customer Contacts

Phone
888-272-1001

Device Sizes

Type Value Unit Text
Outer Diameter 0.035 Inch
Length 150 Centimeter