FDA UDI In Commercial Distribution 🇺🇸 United States

Woven Phillips Follower Urethral Bougie

DI: 00801741073281 · Model: 024010 · C. R. Bard, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Woven Phillips Follower Urethral Bougie
Primary DI
00801741073281
Version / Model
024010
Catalog Number
024010
Company Name
C. R. Bard, Inc.
Labeler DUNS
016898496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-04
Public Version
1
Public Version Date
2020-09-14
Public Version Status
New
Public Device Record Key
d993380c-f967-4912-b8ce-53bc0dd7f99c

Device Description

Woven Phillips Follower Urethral Bougie

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FBW FILIFORM AND FILIFORM FOLLOWER

GMDN Terms

Code Name
11265 Urethral dilator, reusable

Identifiers

Type ID
Primary 00801741073281

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 10 French