FDA UDI In Commercial Distribution 🇺🇸 United States

URETERO-RENO VIDEOSCOPE

DI: 04953170343582 · Model: OLYMPUS URF-V2 · OLYMPUS MEDICAL SYSTEMS CORP.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
URETERO-RENO VIDEOSCOPE
Primary DI
04953170343582
Version / Model
OLYMPUS URF-V2
Company Name
OLYMPUS MEDICAL SYSTEMS CORP.
Labeler DUNS
711789789
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
8
Public Version Date
2023-01-16
Public Version Status
Update
Public Device Record Key
55443ed9-5b12-4fdf-976b-6f064c13966e

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
FGB Ureteroscope and accessories, flexible/rigid
NWB Endoscope, accessories, narrow band spectrum

GMDN Terms

Code Name
38703 Flexible video ureterorenoscope, reusable

Identifiers

Type ID
Primary 04953170343582

Customer Contacts