FDA UDI In Commercial Distribution 🇺🇸 United States

Cystoscopy instrument

DI: 04059082025872 · Model: 395 400 020 · SOPRO-COMEG GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cystoscopy instrument
Primary DI
04059082025872
Version / Model
395 400 020
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
2019-08-21
Public Version Status
Update
Public Device Record Key
5445fb17-806c-4eee-b81a-ac5cb7d7aec7

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
35080 Rigid endoscopic tissue manipulation forceps, reusable

Identifiers

Type ID
Primary 04059082025872

Premarket Submissions

Submission Number Supplement Number
K945262 000