FDA UDI In Commercial Distribution 🇺🇸 United States

Proxis™ Ureteral Access Sheath

DI: 00801741101694 · Model: 231045 · C. R. Bard, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Proxis™ Ureteral Access Sheath
Primary DI
00801741101694
Version / Model
231045
Catalog Number
231045
Company Name
C. R. Bard, Inc.
Labeler DUNS
016898496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-26
Public Version
4
Public Version Date
2020-12-21
Public Version Status
Update
Public Device Record Key
a89a17ca-4031-4ab1-93cd-6d0917e9b911

Device Description

Proxis™ Ureteral Access Sheath

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FED endoscopic access overtube, gastroenterology-urology

GMDN Terms

Code Name
64309 Ureteral sheath

Identifiers

Type ID
Primary 00801741101694

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 12 French
Length 45 Centimeter