FDA UDI In Commercial Distribution 🇺🇸 United States

Revita® Guidewire

DI: 00816349014833 · Model: FRABF-001V · Lake Region Medical
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Revita® Guidewire
Primary DI
00816349014833
Version / Model
FRABF-001V
Catalog Number
50110
Company Name
Lake Region Medical
Labeler DUNS
031108704
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-16
Public Version
1
Public Version Date
2024-12-24
Public Version Status
New
Public Device Record Key
b5cf7966-2ea9-46f2-94b9-8421f1d53632

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
KNT Tubes, Gastrointestinal (And Accessories)

GMDN Terms

Code Name
46691 Gastro-urological guidewire, single-use

Identifiers

Type ID
Primary 00816349014833
Package 10816349014830

Device Sizes

Type Value Unit Text
Guidewire Length 450 Centimeter
Guidewire Diameter 0.35 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry, KEep away from sunlight