FDA UDI In Commercial Distribution 🇺🇸 United States

Percuflex™

DI: 08714729040361 · Model: M0061453690 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Percuflex™
Primary DI
08714729040361
Version / Model
M0061453690
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
021717889
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
ac79eea6-38b6-45b1-bfbc-7fcf0e099745

Device Description

Ureteral Stent

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
MR Safe
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
FAD STENT, URETERAL

GMDN Terms

Code Name
58005 Polymeric ureteral stent

Identifiers

Type ID
Primary 08714729040361

Device Sizes

Type Value Unit Text
Device Size Text, specify 7 F Stent Diameter
Device Size Text, specify 20 cm Effective Length
Device Size Text, specify 2.3 mm Stent Diameter