FDA UDI In Commercial Distribution 🇺🇸 United States

Flex-X

DI: 04048551278239 · Model: 11278VU · Karl Storz GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Flex-X
Primary DI
04048551278239
Version / Model
11278VU
Company Name
Karl Storz GmbH & Co. KG
Labeler DUNS
315731430
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
a496452b-9ad2-4ca4-9a30-c26b286e1d01

Device Description

Video Uretero-Renoscope, FLEX-X C

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Ethylene Oxide", "Hydrogen Peroxide", "Liquid Chemical", "Peracetic Acid"]

Product Codes

Code Name
FGB Ureteroscope and accessories, flexible/rigid

GMDN Terms

Code Name
38703 Flexible video ureterorenoscope, reusable

Identifiers

Type ID
Primary 04048551278239

Premarket Submissions

Submission Number Supplement Number
K131369 000