FDA UDI Not in Commercial Distribution 🇺🇸 United States

MULTI-FLEX

DI: 00821925001107 · Model: 5477280 · Gyrus Acmi, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MULTI-FLEX
Primary DI
00821925001107
Version / Model
5477280
Company Name
Gyrus Acmi, Inc.
Labeler DUNS
007198742
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-03
Public Version
6
Public Version Date
2023-08-17
Public Version Status
Update
Public Device Record Key
3feb7520-c920-4360-ae51-e6bf8dc10dfd
Distribution End Date
2017-06-15

Device Description

MULTI-FLEX Open Tip Ureteral Stent 7.0 FR X 28 cm w/PTFE Moveable Core Guidewire .038" X 150 cm w/5 FR Open-End Ureteral Catheter

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
FAD STENT, URETERAL

GMDN Terms

Code Name
58005 Polymeric ureteral stent

Identifiers

Type ID
Primary 00821925001107

Premarket Submissions

Submission Number Supplement Number
K930733 000