FDA UDI In Commercial Distribution 🇺🇸 United States

Cystoscope

DI: 04059082004112 · Model: 165 293 002BC001 · SOPRO-COMEG GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cystoscope
Primary DI
04059082004112
Version / Model
165 293 002BC001
Company Name
SOPRO-COMEG GmbH
Labeler DUNS
507185952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-22
Public Version
4
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
40e1f843-4d4d-4a94-b8a8-e554bb5a8575

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FAJ Cystoscope and accessories, flexible/rigid

GMDN Terms

Code Name
17145 Rigid optical cystoscope

Identifiers

Type ID
Primary 04059082004112

Premarket Submissions

Submission Number Supplement Number
K945262 000