FDA UDI In Commercial Distribution 🇺🇸 United States

Revere Hybrid Access Catheter

DI: 00840303712725 · Model: REVERE6F55 · BALT USA LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Revere Hybrid Access Catheter
Primary DI
00840303712725
Version / Model
REVERE6F55
Catalog Number
N/A
Company Name
BALT USA LLC
Labeler DUNS
945543689
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-14
Public Version
1
Public Version Date
2024-08-22
Public Version Status
New
Public Device Record Key
c6e9fd57-e4af-4c8e-a48e-88071bea84e3

Device Description

Revere Hybrid Access Catheter is a single lumen, hybrid coil and braid-reinforced, variable stiffness catheter with a radiopaque zone on the distal end and a luer hub on the proximal end. The catheter is provided sterile, non-pyrogenic, and is intended for single use only.

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
DQY Catheter, Percutaneous

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Primary 00840303712725

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K182918 000

Device Sizes

Type Value Unit Text
Catheter Working Length 55 Centimeter
Device Size Text, specify 70 cm Dilator

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dry place at room temperature and away from light