FDA UDI In Commercial Distribution 🇺🇸 United States

Flex-X

DI: 04048551226353 · Model: 11278AC1 · 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
04048551226353
Version / Model
11278AC1
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
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
5c2bd02b-6074-4113-9a1a-d9ff91b89dc3

Device Description

Pediat. Cysto-Urethro-Fiberscope, FELX-X

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
["Hydrogen Peroxide", "Liquid Chemical", "Peracetic Acid", "Ethylene Oxide"]

Product Codes

Code Name
FGB Ureteroscope and accessories, flexible/rigid

GMDN Terms

Code Name
36632 Flexible fibreoptic cystourethroscope

Identifiers

Type ID
Primary 04048551226353

Premarket Submissions

Submission Number Supplement Number
K982905 000