FDA UDI In Commercial Distribution 🇺🇸 United States

Urethrotomy sheath

DI: 04059082010991 · Model: 199 110 080BC · SOPRO-COMEG GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Urethrotomy sheath
Primary DI
04059082010991
Version / Model
199 110 080BC
Company Name
SOPRO-COMEG GmbH
Labeler DUNS
507185952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-12
Public Version
5
Public Version Date
2019-03-11
Public Version Status
Update
Public Device Record Key
98db12b3-b407-4a29-b235-928f7fe146dc

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
EZO Urethrotome

GMDN Terms

Code Name
37086 Endoscope sheath, reusable

Identifiers

Type ID
Primary 04059082010991

Premarket Submissions

Submission Number Supplement Number
K971881 000